Thomas Liehr
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Biology
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(Suggest an Edit or Addition)Thomas Liehr's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo (2008) (348)
- Small supernumerary marker chromosomes (sSMC) in humans (2004) (280)
- Microdissection based high resolution multicolor banding for all 24 human chromosomes. (2002) (231)
- Aneuploidy and Confined Chromosomal Mosaicism in the Developing Human Brain (2007) (220)
- Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish (2015) (213)
- Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. (2007) (205)
- Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: Differential expression and pathological meaning (2009) (195)
- Microdeletion and Microduplication Syndromes (2012) (171)
- Genome‐wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U‐CH1 (2001) (163)
- Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation (2005) (163)
- Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification (2003) (159)
- A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) (2001) (158)
- Complex chromosomal rearrangements: origin and meiotic behavior. (2011) (142)
- Human male recombination maps for individual chromosomes. (2004) (142)
- Fluorescence In Situ Hybridization (FISH) — Application Guide (2009) (142)
- PDE3A mutations cause autosomal dominant hypertension with brachydactyly (2015) (139)
- Localization of the human beta-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development. (1994) (136)
- Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones. (2010) (125)
- Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. (2009) (122)
- Cytogenetic contribution to uniparental disomy (UPD) (2010) (117)
- Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. (2010) (115)
- Widespread expression of the peripheral myelin protein‐22 gene (pmp22) in neural and non‐neural tissues during murine development (1995) (113)
- Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis (2003) (111)
- Molecular Definition of High-resolution Multicolor Banding Probes: First Within the Human DNA Sequence Anchored FISH Banding Probe Set (2008) (105)
- The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1 (2008) (97)
- Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements (2002) (93)
- Rapid detection of subtelomeric deletion/duplication by novel real‐time quantitative PCR using SYBR‐green dye (2004) (92)
- X chromosome aneuploidy in the Alzheimer’s disease brain (2014) (89)
- Small Supernumerary Marker Chromosomes (sSMC) (2012) (85)
- A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH) (1992) (85)
- Multicolor FISH probe sets and their applications. (2004) (84)
- Patterns of genomic imbalances in human solid tumors (Review). (2000) (83)
- Variation in MLH1 distribution in recombination maps for individual chromosomes from human males. (2006) (83)
- Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB) (2006) (81)
- Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3–q25.2 and mutation analysis (1998) (76)
- Chromosome distribution in human sperm – a 3D multicolor banding-study (2008) (76)
- Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation‐specific PCR (2006) (75)
- Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure. (2005) (73)
- Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisation. (1998) (70)
- Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries (2002) (65)
- The DNA-based structure of human chromosome 5 in interphase. (2002) (65)
- Small Supernumerary Marker Chromosomes and Uniparental Disomy Have a Story to Tell (2011) (62)
- Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding (2006) (60)
- Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB) (2001) (60)
- Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity. (2007) (59)
- LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells (2018) (58)
- Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. (2003) (57)
- Current developments in human molecular cytogenetic techniques. (2002) (57)
- Common Fragile Sites: Genomic Hotspots of DNA Damage and Carcinogenesis (2012) (57)
- Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. (1997) (56)
- New eukaryotic semaphorins with close homology to semaphorins of DNA viruses. (1998) (55)
- Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathway (2014) (55)
- Handling small supernumerary marker chromosomes in prenatal diagnostics (2009) (54)
- Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues (2010) (54)
- The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells (2005) (53)
- Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. (2008) (53)
- First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding (2013) (53)
- Systems genetics view of endometriosis: a common complex disorder. (2015) (52)
- Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level (2005) (52)
- Small Supernumerary Marker Chromosomes (sSMC): A Guide for Human Geneticists and Clinicians (2011) (51)
- Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion (1996) (51)
- DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome. (2016) (50)
- Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study (2013) (50)
- Ten years follow up of a boy with a complex chromosomal rearrangement: Going from a > 5 to 15‐breakpoint CCR (2003) (48)
- Comparative Chromosomal Mapping of Microsatellites in Leporinus Species (Characiformes, Anostomidae): Unequal Accumulation on the W Chromosomes (2013) (48)
- Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes (2010) (47)
- Array painting using microdissected chromosomes to map chromosomal breakpoints (2007) (47)
- Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. (2004) (47)
- The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2 (2013) (47)
- Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method (2004) (46)
- FISH banding methods: applications in research and diagnostics (2002) (45)
- Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases (2001) (44)
- Next generation phenotyping in Emanuel and Pallister‐Killian syndrome using computer‐aided facial dysmorphology analysis of 2D photos (2018) (44)
- Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. (2008) (43)
- The Human Genome Puzzle – the Role of Copy Number Variation in Somatic Mosaicism (2010) (43)
- Emerging patterns of genome organization in Notopteridae species (Teleostei, Osteoglossiformes) as revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH) (2019) (42)
- FISH analysis of interphase nuclei extracted from paraffin-embedded tissue. (1995) (42)
- Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes (2002) (41)
- Small supernumerary marker chromosomes and their correlation with specific syndromes (2015) (41)
- Monitoring of gas station attendants exposure to benzene, toluene, xylene (BTX) using three-color chromosome painting (2014) (41)
- Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review (2000) (41)
- Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype – 17 New Cases and a Review of the Literature (2008) (40)
- Genetic imbalances in 26 cases of penile squamous cell carcinoma (2001) (40)
- Chromosome variability of human multipotent mesenchymal stromal cells (2007) (39)
- Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples. (2003) (39)
- Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and fox (2000) (39)
- Heterogenic molecular basis for loss of ABL1‐BCR transcription: Deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR‐ABL1‐positive chronic myeloid leukemia (2002) (39)
- Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level. (2008) (39)
- A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1—evidence for high variability in mosaicism in different tissues of sSMC carriers (2007) (39)
- Variation in crossover interference levels on individual chromosomes from human males. (2008) (39)
- Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature (2007) (38)
- Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them (2008) (38)
- Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unravelling the full complexity of multi-factorial multidrug resistance (2016) (38)
- Typical and partial cat eye syndrome: identification of the marker chromosome by FISH (1992) (38)
- Heteromorphic variants of chromosome 9 (2013) (37)
- Rapid Prenatal Diagnostics in the Interphase Nucleus: Procedure and Cut-off Rates (2005) (37)
- Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae) (2016) (36)
- Chromosomal Mapping of Repetitive DNAs in Triportheus trifurcatus (Characidae, Characiformes): Insights into the Differentiation of the Z and W Chromosomes (2014) (36)
- Karyotyping of human synaptonemal complexes by cenM-FISH (2003) (36)
- Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes (2012) (36)
- Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. (2003) (35)
- 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families (2010) (35)
- Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae) (2013) (34)
- X‐linked intellectual disability related genes disrupted by balanced X‐autosome translocations (2015) (34)
- An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. (2007) (34)
- Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases. (2005) (33)
- Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes. (2006) (33)
- 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2 (2012) (32)
- Localization of mariner DNA transposons in the human genome by PRINS. (1999) (32)
- Small Supernumerary Marker Chromosomes in Human Infertility (2015) (32)
- Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon (2008) (32)
- Complex small supernumerary marker chromosomes – an update (2013) (32)
- Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity? (2008) (32)
- Tracking the evolutionary pathway of sex chromosomes among fishes: characterizing the unique XX/XY1Y2 system in Hoplias malabaricus (Teleostei, Characiformes) (2018) (31)
- Suspension (S)-FISH, a New Technique for Interphase Nuclei (2002) (31)
- Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH) (2014) (31)
- Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report (2012) (31)
- Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter (2003) (31)
- Evolutionary Dynamics of rDNAs and U2 Small Nuclear DNAs in Triportheus (Characiformes, Triportheidae): High Variability and Particular Syntenic Organization. (2017) (31)
- Independent Sex Chromosome Evolution in Lower Vertebrates: A Molecular Cytogenetic Overview in the Erythrinidae Fish Family (2013) (31)
- Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker (2001) (31)
- Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpoints. (2007) (31)
- Altered tissue distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-DNA adducts in mice transgenic for human sulfotransferases 1A1 and 1A2. (2011) (30)
- FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male (2004) (30)
- Analysis of non-crossover bivalents in pachytene cells from 10 normal men. (2006) (30)
- Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics. (2008) (30)
- Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation (2003) (30)
- Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males. (2005) (29)
- Fluorescence In Situ Hybridization (FISH) (2017) (29)
- Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia‐negative chronic myelogenous leukaemia (2001) (29)
- Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma (1999) (29)
- Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC (2006) (29)
- The use of array-CGH in a cohort of Greek children with developmental delay (2010) (29)
- Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review (2007) (28)
- Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line (2006) (28)
- t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. (2007) (28)
- Tetrasomy 8 as a clonal anomaly in myeloid neoplasias. (1994) (27)
- Impact of Various Parameters in Detecting Chromosomal Aberrations by FISH to Describe Radiosensitivity (2004) (27)
- Evolution versus constitution: differences in chromosomal inversion (2005) (26)
- Is 24-Color FISH Detection of In-Vitro Radiation-Induced Chromosomal Aberrations Suited to Determine Individual Intrinsic Radiosensitivity? (2002) (26)
- Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes (2011) (26)
- A report of pure 7p duplication syndrome and review of the literature (2006) (26)
- Genotype/phenotype analysis in a patient with pure and complete trisomy 12p (2004) (26)
- Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation? (2019) (26)
- Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species (2011) (25)
- Partial hexasomy 15pter→15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report (2003) (25)
- Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines (1999) (25)
- X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation (2010) (25)
- A molecular cytogenetic study of chromosome evolution in chimpanzee (2005) (25)
- New insights into the evolution of chromosome 1 (2004) (25)
- A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes. (2010) (25)
- Structure and chromosomal localization of the human and mouse muscle fructose-1,6-bisphosphatase genes. (2000) (25)
- Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis. (2002) (25)
- Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8,18, and 21 in three patients (2010) (25)
- Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. (2005) (25)
- Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. (2005) (24)
- Chromosomal evolution in naked catfishes (Bagridae, Siluriformes): A comparative chromosome mapping study (2014) (24)
- Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae) (2014) (24)
- Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences (2005) (24)
- New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites. (2009) (24)
- Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. (2009) (24)
- Genomic gain of the epidermal growth factor receptor harboring band 7p12 is part of a complex pattern of genomic imbalances in oral squamous cell carcinomas. (2004) (24)
- A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24→1q22 and partial monosomy 4q27→q28 (2003) (24)
- Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter → p12.2)[10] (2003) (24)
- Unexpected results in the constitution of small supernumerary marker chromosomes. (2012) (24)
- Cytogenetics, genomics and biodiversity of the South American and African Arapaimidae fish family (Teleostei, Osteoglossiformes) (2019) (24)
- High-throughput sequencing of microdissected chromosomal regions (2010) (24)
- W Chromosome Dynamics in Triportheus Species (Characiformes, Triportheidae): An Ongoing Process Narrated by Repetitive Sequences. (2016) (23)
- Centromere activity in dicentric small supernumerary marker chromosomes (2010) (23)
- Frequent gains and losses of specific chromosome segments in human ovarian carcinomas shown by comparative genomic hybridization. (1997) (23)
- Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies (2006) (23)
- A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation (2008) (23)
- Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation (2006) (23)
- Molecular cytogenetic characterization of epithelioid hemangioendothelioma. (2011) (23)
- Small supernumerary marker chromosomes: A legacy of trisomy rescue? (2018) (23)
- Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia (2008) (23)
- Evidence for multi-copy Mega-NUMTs in the human genome (2021) (23)
- Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements (2014) (23)
- Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions (2009) (23)
- Multicolor FISH methods in current clinical diagnostics (2013) (22)
- FISH on Chromosome Preparations of Peripheral Blood (2002) (22)
- Uniparental Disomy (UPD) in Clinical Genetics (2014) (22)
- Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants (2016) (22)
- First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7 (2009) (22)
- Comparative Cytogenetics and Neo-Y Formation in Small-Sized Fish Species of the Genus Pyrrhulina (Characiformes, Lebiasinidae) (2019) (21)
- Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3. (1999) (21)
- Landscape of snake’ sex chromosomes evolution spanning 85 MYR reveals ancestry of sequences despite distinct evolutionary trajectories (2020) (21)
- Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer (2018) (21)
- Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations (1997) (21)
- Noninvasive Prenatal Testing - When Is It Advantageous to Apply (2017) (21)
- The hierarchically organized splitting of chromosomal bands for all human chromosomes (2009) (21)
- Paternal uniparental isodisomy for chromosome 14 with mosaicism for a supernumerary marker chromosome 14 (2007) (21)
- New insights into the karyotypic evolution in muroid rodents revealed by multicolor banding applying murine probes (2010) (20)
- New cytogenetically visible copy number variant in region 8q21.2 (2011) (20)
- Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensis (2017) (20)
- Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair (2010) (20)
- Residual Chromosomal Damage after Radiochemotherapy with and without Amifostine Detected by 24-Color FISH (2003) (20)
- Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations. (2015) (20)
- A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype. (2014) (20)
- Distal partial trisomy 1q: report of two cases and a review of the literature (2007) (20)
- Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations (2003) (20)
- Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia (2012) (20)
- Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13. (1998) (20)
- Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. (2011) (20)
- A definition for cytogenomics - Which also may be called chromosomics (2021) (19)
- 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences (2009) (19)
- A New Multicolor Fluorescence In Situ Hybridization Probe Set Directed Against Human Heterochromatin (2012) (19)
- Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing (2016) (19)
- A supernumerary “B-sex” chromosome drives male sex determination in the Pachón cavefish, Astyanax mexicanus (2021) (19)
- Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8 (1999) (19)
- Maternal insertion of 18q11.2–q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB) (2001) (19)
- Small Supernumerary Marker Chromosomes (sSMCs): A Spotlight on Some Nomenclature Problems (2009) (19)
- High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia (2015) (19)
- A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male. (2009) (19)
- The current state of molecular cytogenetics in cancer diagnosis (2015) (19)
- Human Ring Chromosomes – New Insights for their Clinical Significance (2013) (19)
- Overview of currently available approaches used in cytogenomics (2021) (19)
- An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome‐like phenotype in a female patient (2010) (19)
- CD8 Locus Nuclear Dynamics during Thymocyte Development (2010) (19)
- A Highly Complex Chromosomal Rearrangement between Five Chromosomes in a Healthy Female Diagnosed in Preparation for Intracytoplasmatic Sperm Injection (2005) (19)
- Evidence for a new microdeletion syndrome in 15q21. (2003) (19)
- Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11→q11:)/46,XX karyotype (2002) (19)
- De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature (2004) (19)
- Chromosomal Evolution and Evolutionary Relationships of Lebiasina Species (Characiformes, Lebiasinidae) (2019) (19)
- A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis (2002) (18)
- Comprar Fluorescence In Situ Hybridization (FISH) - Application Guide | Liehr, Thomas | 9783540705802 | Springer (2009) (18)
- Recommendations for whole genome sequencing in diagnostics for rare diseases (2022) (18)
- Molecular Cytogenetics: The Standard FISH and PRINS Procedure (2009) (18)
- Characterization of the mouse liver fructose-1,6-bisphosphatase gene. (2001) (18)
- Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells. (2001) (18)
- Detection and Correlation of Single and Concomitant TP53, PTEN, and CDKN2A Alterations in Gliomas (2019) (18)
- Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review (2019) (18)
- Comparison of the three rat GDP‐L‐fucose:β‐D‐galactoside 2‐α‐L‐fucosyltransferases FTA, FTB and FTC (2001) (18)
- Increased Efficiency of Fluorescence In Situ Hybridization (FISH) Using the Microwave (2005) (17)
- Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family. (2014) (17)
- Deletion monitoring in skin tumors by interphase-FISH using band-specific DNA probes. (1999) (17)
- Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin (2012) (17)
- Two‐Photon Multicolor FISH: A Versatile Technique to Detect Specific Sequences with in Single DNA Molecules in Cells and Tissues (2000) (17)
- Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes) (2020) (17)
- Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics (2012) (17)
- Chromosomal Composition of Micronuclei in Human Leukocytes Exposed to Mitomycin C (2012) (17)
- Comparative interphase cytogenetics using FISH on human ovarian carcinomas. (1994) (17)
- Narrowing the deleted region associated with the 15q21 syndrome. (2005) (17)
- Characterization of sSMC by FISH and molecular techniques. (2011) (17)
- Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. (2007) (17)
- A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics (2008) (17)
- First Chromosomal Analysis in Hepsetidae (Actinopterygii, Characiformes): Insights into Relationship between African and Neotropical Fish Groups (2017) (17)
- First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae) (2013) (17)
- Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies (2008) (17)
- Prenatal screening of cytogenetic anomalies – a Western Indian experience (2015) (16)
- Inactivation of AMMECR1 is associated with growth, bone, and heart alterations (2018) (16)
- A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. (2013) (16)
- Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl (2010) (16)
- An unexpected finding in a child with neurological problems: mosaic ring chromosome 18 (2008) (16)
- Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human (2017) (16)
- Comparative cytogenetics in the genus Hoplias (Characiformes, Erythrinidae) highlights contrasting karyotype evolution among congeneric species (2015) (16)
- Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibers. (1997) (16)
- Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines (2006) (16)
- From Chromosomes to Genome: Insights into the Evolutionary Relationships and Biogeography of Old World Knifefishes (Notopteridae; Osteoglossiformes) (2018) (16)
- First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15‐16 (2003) (16)
- Molecular Cytogenetic Characterization of the Human Cerebral Microvessel Endothelial Cell Line hCMEC/D3 (2009) (16)
- Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei (2002) (16)
- European registration process for Clinical Laboratory Geneticists in genetic healthcare (2017) (16)
- An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis (2010) (16)
- Sex Differences in Diabetes- and TGF-β1-Induced Renal Damage (2020) (16)
- A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected]. (2003) (16)
- DNA Copy Number Variations as Markers of Mutagenic Impact (2019) (16)
- Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature (2010) (16)
- Repetitive elements, heteromorphisms, and copy number variants (2021) (16)
- Deciphering the Origin and Evolution of the X1X2Y System in Two Closely-Related Oplegnathus Species (Oplegnathidae and Centrarchiformes) (2019) (15)
- Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. (2009) (15)
- Characterisation of Small Supernumerary Marker Chromosomes (sSMC) in Human (2004) (15)
- A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case (2012) (15)
- BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients (2016) (15)
- Chromosomal heterogeneity of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH). (1993) (15)
- The Standard FISH Procedure (2017) (15)
- Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature (2008) (15)
- Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches. (2006) (15)
- Chromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories (2020) (15)
- Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes (2008) (15)
- Mouse white adipose tissue‐derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation (2015) (15)
- Parental origin of deletions and duplications – about the necessity to check for cryptic inversions (2018) (15)
- Tetrasomy 9p Mosaicism Associated with a Normal Phenotype in Two Cases (2012) (15)
- Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements (2011) (15)
- Analysis of the histone cluster in Senegalese sole (Solea senegalensis): evidence for a divergent evolution of two canonical histone clusters. (2017) (15)
- Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints. (2004) (15)
- DNA degradation during maturation of erythrocytes – molecular cytogenetic characterization of Howell-Jolly bodies (2007) (15)
- UKCCCR guidelines for the use of cell lines in cancer research (1999) (15)
- Evolution of the Proto Sex-Chromosome in Solea senegalensis (2019) (14)
- A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3 (2010) (14)
- Interphase cytogenetics by fish on archival paraffin material and cultured-cells on human ovarian-tumors. (1994) (14)
- Cytogenetic mechanisms of unisexuality in rock lizards (2020) (14)
- Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports (2017) (14)
- An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA) (2000) (14)
- Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male (2009) (14)
- Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis (2018) (14)
- Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding (2005) (14)
- Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. (2007) (14)
- A Neocentric Isochromosome Yp Present as Additional Small Supernumerary Marker Chromosome – Evidence against U-Type Exchange Mechanism? (2009) (14)
- A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report (2009) (14)
- The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity. (2007) (14)
- Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case. (2014) (13)
- Another Small Supernumerary Marker Chromosome (sSMC) Derived from Chromosome 2: Towards a Genotype/Phenotype Correlation (2005) (13)
- Impaired Spermatogenesis due to Small Supernumerary Marker Chromosomes: The Reason for Infertility Is Only Reliably Ascertainable by Cytogenetics (2018) (13)
- Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances (2011) (13)
- Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay (2005) (13)
- Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomes. (2015) (13)
- Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians? (2021) (13)
- Deciphering the Evolutionary History of Arowana Fishes (Teleostei, Osteoglossiformes, Osteoglossidae): Insight from Comparative Cytogenomics (2019) (13)
- Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patient (2013) (13)
- Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success. (2007) (13)
- Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias. (2000) (12)
- Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by indocyanine green in breast adenocarcinoma MCF-7 cells. (2013) (12)
- Partial trisomy of distal 19q detected by quantitative real‐time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay (2007) (12)
- New Immortalized Cell Lines of Patients With Small Supernumerary Marker Chromosome (2007) (12)
- Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae) (2020) (12)
- POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism. (2010) (12)
- In vitro cytotoxicity and genotoxicity studies of gold nanoparticles-mediated photo-thermal therapy versus 5-fluorouracil (2015) (12)
- Centromere-Specific Multicolor-FISH (cenM-FISH) (2002) (12)
- Molecular cytogenetic characterisation of the colorectal cancer cell line SW480. (2004) (12)
- Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18 (2007) (12)
- A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues. (1996) (12)
- Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome (2015) (12)
- Nucleus extraction from single mounted tissue sections. (1999) (12)
- Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy (2009) (12)
- A First Generation Comparative Chromosome Map between Guinea Pig (Cavia porcellus) and Humans (2015) (12)
- Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males (2007) (12)
- Chromosomes in a genome-wise order: evidence for metaphase architecture (2016) (12)
- How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set (2012) (12)
- Repetitive Elements in Humans (2021) (12)
- Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. (2003) (12)
- From Human Cytogenetics to Human Chromosomics (2019) (12)
- An Insight into the Chromosomal Evolution of Lebiasinidae (Teleostei, Characiformes) (2020) (12)
- Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report. (2010) (11)
- The peripheral myelin protein 22 kDa (PMP22) gene is amplified in cell lines derived from glioma and osteogenic sarcoma. (1997) (11)
- Small supernumerary marker chromosomes and the nuclear architecture of sperm – a study in a fertile and an infertile brother (2015) (11)
- Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries (2019) (11)
- Pitfalls of rapid prenatal diagnosis using the interphase nucleus (2001) (11)
- Interchromosomal interactions with meaning for disease (2021) (11)
- Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytes (2016) (11)
- Integrative genetic map of repetitive DNA in the sole Solea senegalensis genome shows a Rex transposon located in a proto-sex chromosome (2019) (11)
- Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception? (2018) (11)
- Microdissection-derived Murine Mcb Probes from Somatic Cell Hybrids (2005) (11)
- Reorganization of inter‐chromosomal interactions in the 2q37‐deletion syndrome (2018) (11)
- A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion. (2014) (11)
- Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex (2016) (11)
- Precise breakpoint characterization of the colon adenocarcinoma cell line HT‐29 clone 19A by means of 24‐color fluorescence in situ hybridization and multicolor banding (2003) (11)
- Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors. (2012) (11)
- Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stages. (1998) (11)
- International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts (2021) (10)
- A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia (2014) (10)
- Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH). (2008) (10)
- First Molecular Cytogenetic Characterization of Murine Malignant Mesothelioma Cell Line AE17 and In Silico Translation to the Human Genome (2017) (10)
- New Insights Into Chromomere Organization Provided by Lampbrush Chromosome Microdissection and High-Throughput Sequencing (2020) (10)
- Identification of novel drug resistance mechanisms by genomic and transcriptomic profiling of glioblastoma cells with mutation-activated EGFR. (2021) (10)
- Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma (2015) (10)
- Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas (2003) (10)
- Mitotic Stability of Small Supernumerary Marker Chromosomes: A Study Based on 93 Immortalized Cell Lines (2014) (10)
- Pre- and Postnatal Diagnostics and Research on Peripheral Blood, Bone Marrow, Chorion, Amniocytes, and Fibroblasts (2017) (10)
- Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells (2009) (10)
- Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family (2019) (10)
- Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. (2003) (10)
- Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches. (2003) (10)
- CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes (2016) (10)
- Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines (2003) (10)
- Genome and Phylogenetic Analysis of Genes Involved in the Immune System of Solea senegalensis – Potential Applications in Aquaculture (2019) (10)
- Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation (2009) (10)
- Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes. (2006) (9)
- Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization. (2010) (9)
- Chromosomes of Asian cyprinid fishes: cytogenetic analysis of two representatives of small paleotetraploid tribe Probarbini (2018) (9)
- Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome. (2008) (9)
- “Classical cytogenetics” is not equal to “banding cytogenetics” (2017) (9)
- Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis. (2018) (9)
- First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease (2016) (9)
- Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes (2017) (9)
- New Insights into Phasmatodea Chromosomes (2017) (9)
- Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. (2008) (9)
- Detection of Cyto- and Genotoxicity of Rod-Shaped Gold Nanoparticles in Human Blood Lymphocytes Using Comet-FISH (2015) (9)
- Premature Ovarian Failure Caused by a Heterozygous Missense Mutation in POF1B and a Reciprocal Translocation 46,X,t(X;3)(q21.1;q21.3) (2015) (9)
- A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding. (2002) (9)
- Parental origin and functional relevance of a de novo UBE3A variant. (2011) (9)
- Exploring Supernumeraries - A New Marker for Screening of B-Chromosomes Presence in the Yellow Necked Mouse Apodemus flavicollis (2016) (9)
- Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis (2011) (9)
- Detection of microdeletions in the short arm of the X chromosome by chromosome stretching (2002) (9)
- I-FISH control of CGH-detected gain of DNA sequence copy number in oral squamous cell carcinomas (OSCC). (2000) (9)
- Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome (2001) (9)
- Determination by interphase-FISH of the clonality of aberrant karyotypes in human hematopoietic neoplasias. (1995) (9)
- Molecular–cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs) (2004) (9)
- CGH-detected DNA sequence copy number amplifications can be confirmed by interphase-FISH: new possiblities for prognostic approaches in oral squamous cell carcinomas. (1998) (9)
- The applicability of interphase chromosome-specific multicolor banding (ICS-MCB) for studying neurodevelopmental and neurodegenerative disorders (2019) (9)
- Duplication 4q associated with chronic cholestatic changes in liver biopsy. (2010) (9)
- Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient (2005) (9)
- The Amazonian Red Side-Necked Turtle Rhinemys rufipes (Spix, 1824) (Testudines, Chelidae) Has a GSD Sex-Determining Mechanism with an Ancient XY Sex Microchromosome System (2020) (9)
- Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1–11.2;p13.3) (2007) (9)
- Small supernumerary marker chromosomes detected in connection with infertility. (2014) (8)
- Deletion 2q31.2‐q31.3 in a 4‐year‐old girl with microcephaly and severe mental retardation (2011) (8)
- Hypermethylation in Gene Promoters Are Induced by Chronic Exposure to Benzene, Toluene, Ethylbenzene and Xylenes. (2020) (8)
- Does positioning of chromosomes 8 and 21 in interphase drive t(8;21) in acute myelogenous leukemia? (2012) (8)
- Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability (2020) (8)
- Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report (2009) (8)
- Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes (2019) (8)
- New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome. (2005) (8)
- Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting (2016) (8)
- Interspecific Genetic Differences and Historical Demography in South American Arowanas (Osteoglossiformes, Osteoglossidae, Osteoglossum) (2019) (8)
- Analysis of copy number variations induced by ultrashort electron beam radiation in human leukocytes in vitro (2019) (8)
- Molecular Cytogenetic Characterization of Two Murine Colorectal Cancer Cell Lines (2018) (8)
- Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH. (1999) (8)
- First chromosomal analysis in Gymnarchus niloticus (Gymnarchidae: Osteoglossiformes): insights into the karyotype evolution of this ancient fish order (2018) (8)
- Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH (1995) (8)
- Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome. (2009) (8)
- Three Cases with Enlarged Acrocentric p-arms and Two Cases with Cryptic Partial Trisomies (2005) (8)
- Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors (2015) (8)
- Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. (2012) (8)
- Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus Macrobrachium (Crustacea: Decapoda: Palaemonidae) (2020) (8)
- Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report (2009) (8)
- In Silico Detection and FISH Analysis to Determine Location of miRNAs in Solea Senegalensis Chromosomes Using BACs (2018) (8)
- Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. (2005) (8)
- Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH (2009) (8)
- The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility? (2010) (8)
- Screening of phytochemicals and toxicity of medicinal plants, Dillenia species, reveals potential natural product resources (2017) (8)
- Genomic Organization of Repetitive DNA Elements and Extensive Karyotype Diversity of Silurid Catfishes (Teleostei: Siluriformes): A Comparative Cytogenetic Approach (2019) (8)
- Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient (2013) (7)
- Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1. (2001) (7)
- Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients. (2019) (7)
- Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18 – how to counsel? (2012) (7)
- Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2) (2004) (7)
- Molecular Cytogenetic Characterization Identified the Murine B-Cell Lymphoma Cell Line A-20 as a Model for Sporadic Burkitt’s Lymphoma (2017) (7)
- Heterochromatic regions in Japanese quail chromosomes: comprehensive molecular-cytogenetic characterization and 3D mapping in interphase nucleus (2019) (7)
- BAC-probes applied for characterization of fragile sites (FS). (2015) (7)
- Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. (2004) (7)
- Evolution of a Multiple Sex-Chromosome System by Three-Sequential Translocations among Potential Sex-Chromosomes in the Taiwanese Frog Odorrana swinhoana (2021) (7)
- Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene (2015) (7)
- Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report (2016) (7)
- An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review (2014) (7)
- Unusual Duplication in the Pericentromeric Region of Chromosome 9 in a Patient with Phenotypic Alterations (2017) (7)
- A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome (2017) (7)
- Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH‐technique (1998) (7)
- Molecular studies reveal a MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype. (2015) (7)
- Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka (2020) (7)
- Small supernumerary marker chromosomes – an update (2014) (7)
- Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay (2016) (7)
- The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB) (2004) (7)
- Spatial organization of fibroblast and spermatocyte nuclei with different B-chromosome content in Korean field mouse, Apodemus peninsulae (Rodentia, Muridae). (2017) (7)
- Influence of aflatoxin B1 on copy number variants in human leukocytes in vitro (2015) (7)
- First postnatal case of mosaic del(22)/r(22) (2003) (7)
- Pre- and Postnatal Diagnostics and Research on Peripheral Blood, Chorion, Amniocytes, and Fibroblasts (2009) (7)
- Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis (2013) (7)
- Chromothripsis Detectable in Small Supernumerary Marker Chromosomes (sSMC) Using Fluorescence In Situ Hybridization (FISH). (2018) (7)
- Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report. (2011) (6)
- Large deletion on the Y-chromosome long arm (Yq) of C57BL/6JBomTac inbred mice (2017) (6)
- Chromosome rearrangements in sublines of human embryonic stem cell lines hESM01 and hESM03 (2013) (6)
- Molecular Cytogenetics in the Era of Chromosomics and Cytogenomic Approaches (2021) (6)
- Chromosomes in the DNA era: Perspectives in diagnostics and research (2019) (6)
- Prenatal Diagnosis and Molecular Cytogenetic Characterization of an Unusual Complex Structural Rearrangement in a Pregnancy Following Intracytoplasmic Sperm Injection (ICSI) (2005) (6)
- Isochromosome 17q in Chronic Lymphocytic Leukemia (2015) (6)
- A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia (2016) (6)
- Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation? (2013) (6)
- Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases. (2009) (6)
- Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents (2014) (6)
- De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features (2014) (6)
- Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases (2013) (6)
- Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8 (2013) (6)
- Human ring chromosomes and small supernumerary marker chromosomes—do they have telomeres? (2012) (6)
- ISH Probes Derived from BACs, Including Microwave Treatment for Better FISH Results (2009) (6)
- A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12). (2012) (6)
- Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm. (2018) (6)
- Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome (2012) (6)
- First Case of Trisomy 13 plus Mosaic Trisomy 1q (2002) (6)
- Mechanisms of Origin and Clinical Effects of Multiple Small Supernumerary Marker Chromosomes, Each Derived from a Different Chromosome (2017) (6)
- Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band). (2010) (6)
- A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5). (2012) (6)
- A novel cytogenetic abnormality t(7;8)(p11.2:q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient (2012) (6)
- Interphase Chromosome-Specific Multicolor Banding (2013) (6)
- Microdissection and whole chromosome painting confirm karyotype transformation in cryptic species of the Lariophagus distinguendus (Förster, 1841) complex (Hymenoptera: Pteromalidae) (2019) (6)
- COMPREHENSIVE MOLECULAR CYTOGENETIC ANALYSIS OF BARBARY MACAQUE ( MACACA SYLVANUS ) (2014) (6)
- Comparison of the three rat GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferases FTA, FTB and FTC. (2001) (6)
- MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report. (2015) (6)
- Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth. (2010) (6)
- FISH Technology (2002) (6)
- Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the Literature (2019) (5)
- A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML (2018) (5)
- BENIGN AND PATHOLOGICAL GAIN OR LOSS OF GENETIC MATERIAL — ABOUT MICROSCOPIC AND SUBMICROSCOPIC COPY NUMBER VARIATIONS (CNVs) IN HUMAN GENETICS. (2016) (5)
- Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens (2015) (5)
- Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature (2014) (5)
- Amplification of protooncogenes in human ovarian carcinomas. (1993) (5)
- New aspects of chromosomal evolution in the gorilla and the orangutan. (2007) (5)
- Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report (2016) (5)
- Chromosome Microdissection on Semi‐Archived Material (2019) (5)
- Characterization of Archived Formalin-Fixed/Paraffin-Embedded or Cryofixed Tissue, Including Nucleus Extraction (2009) (5)
- 43rd Biennial American Cytogenetics Conference. May 4-7, 2014. The Omni Grove Park Inn. Asheville, North Carolina, USA: Abstracts (2014) (5)
- Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy (2017) (5)
- Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma. (2011) (5)
- P 366. 7q11.23 Microduplication Syndrome: Neurophysiological and Neuroradiological Insights into a Rare Chromosomal Disorder (2018) (5)
- Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluation. (2015) (5)
- Molecular cytogenetic characterization of two murine cancer cell lines derived from salivary gland (2018) (5)
- Adding New Pieces to the Puzzle of Karyotype Evolution in Harttia (Siluriformes, Loricariidae): Investigation of Amazonian Species (2021) (5)
- Insertion of the 3' ABL region into the long arm of chromosome 1 in a Philadelphia chromosome-negative chronic myeloid leukemia case. (2010) (5)
- Comparative Chromosomal Studies in Rhinolophus formosae and R. luctus from China and Vietnam: Elevation of R. l. lanosus to Species Rank (2017) (5)
- Tracking the Evolutionary Trends Among Small-Size Fishes of the Genus Pyrrhulina (Characiforme, Lebiasinidae): New Insights From a Molecular Cytogenetic Perspective (2021) (5)
- Conspicuous GTG‐banding results of the centromere‐near region can be caused by alphoid DNA heteromorphism (2003) (5)
- Assignment of the microvascular endothelial differentiation gene 1 (MDG1) to human chromosome band 14q24.2-->q24.3 by fluorescence in situ hybridization. (1997) (5)
- Application of BAC-probes to visualize copy number variants (CNVs). (2015) (5)
- Attrition of X Chromosome Inactivation in Aged Hematopoietic Stem Cells (2021) (5)
- An update on small supernumerary marker chromosomes (sSMC) (2019) (5)
- False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests? (2022) (5)
- Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis (1998) (5)
- A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth (2010) (5)
- Molecular Cytogenetic Characterization of Two Cases with de novo Small Mosaic Supernumerary Marker Chromosomes Derived from Chromosome 16: Towards a Genotype/Phenotype Correlation (2009) (5)
- Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia (2009) (5)
- Verification of Selected Piper Species (Piperaceae) Using Morphological Characters, Molecular Data, and Chemical Constituents (2015) (5)
- Mucopolysaccharidosis III: Molecular basis and treatment. (2021) (5)
- Multiplex FISH and Spectral Karyotyping (2009) (5)
- Characterization of a highly aberrant plasma cell leukemia karyotype: a case report. (2004) (5)
- A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization (2017) (5)
- Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment (2015) (5)
- Against the mainstream: exceptional evolutionary stability of ZW sex chromosomes across the fish families Triportheidae and Gasteropelecidae (Teleostei: Characiformes) (2021) (5)
- A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia. (2016) (5)
- Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report (2008) (5)
- De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report (2014) (5)
- Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population (2020) (5)
- A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21. (2009) (5)
- Extensive Chromosomal Reorganization in Apistogramma Fishes (Cichlidae, Cichlinae) Fits the Complex Evolutionary Diversification of the Genus (2019) (5)
- Involvement of Chromosomes 7, 18 and X in Mitomycin C-Induced Micronuclei (2008) (5)
- Assay of transfection rate in insect cells on a single cell level. (1998) (5)
- Assignment1 of the serologically defined colon cancer antigen 1 gene (SDCCAG1) to human chromosome band 14q22 by in situ hybridization (1999) (5)
- Meiotic synapsis of homeologous chromosomes and mismatch repair protein detection in the parthenogenetic rock lizard Darevskia unisexualis (2021) (5)
- Clinical Impact of Proximal Autosomal Imbalances (2012) (5)
- FISH banding in tumor cytogenetics. (2006) (4)
- Partial Trisomy 2p and Partial Monosomy 2q Arising from a Paternal Intrachromosomal 2q-into-2p Between-Arm Insertion and Paracentric Inversion: Molecular Cytogenetic Characterization of a Four-Break Rearrangement (2013) (4)
- Molecular Cytogenetic Study of the NF2 Gene Deletion in Meningioma in Sudanese Patients (2013) (4)
- Application of Tris-HCl Allows the Specific Labeling of Regularly Prepared Chromosomes by CRISPR-FISH (2020) (4)
- Potential of rod, sphere and semi-cube shaped gold nanoparticles to induce cytotoxicity and genotoxicity in human blood lymphocytes in vitro (2015) (4)
- A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5. (2010) (4)
- Application of yeast artificial chromosomes in fluorescence in situ hybridization. (2006) (4)
- Chromosomal Rearrangements and Origin of the Multiple XX/XY1Y2 Sex Chromosome System in Harttia Species (Siluriformes: Loricariidae) (2022) (4)
- Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation (2015) (4)
- A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences (2008) (4)
- Gene clusters related to metamorphosis in Solea senegalensis are highly conserved. (2020) (4)
- Phenotypic spectrum in uniparental disomy: Low incidence or lack of study? (2013) (4)
- Small Supernumerary Marker Chromosomes and Tumors (2012) (4)
- Uniparental disomy is a chromosomic disorder in the first place (2022) (4)
- Regional localization of rat myelin protein zero Mpz gene to Chromosome 13q24-25 by means of FISH (1995) (4)
- Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case (2014) (4)
- A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature (2003) (4)
- Small supernumerary marker chromosomes 1 with a normal phenotype. (2010) (4)
- Characterization of three small supernumerary marker chromosomes (sSMC) in humans (2013) (4)
- 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature (2016) (4)
- Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives (2020) (4)
- FISH Banding Techniques (2009) (4)
- Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities (2017) (4)
- Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles (2021) (4)
- Association of genome instability and neurodegeneration in the cerebral cortex and hippocampus in Alzheimer's disease brain: Evidences for a new pathogenetic mechanism of the disease (2008) (4)
- Comparative Distribution of Repetitive Sequences in the Karyotypes of Xenopus tropicalis and Xenopus laevis (Anura, Pipidae) (2021) (4)
- Interphase-FISH examinations in paraffin sections from benign, precancerous, and cancerous lesions of the skin and oral mucosa. (1997) (4)
- A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss (2018) (4)
- Clonality determined by fluorescence in situ hybridization of single-cell aberrations in hematopoietic neoplasias. (1999) (4)
- Copy number variations (CNVs) - is there a biological difference between submicroscopic and microscopically visible ones? (2013) (4)
- Identification of metastasis-related genes by genomic and transcriptomic studies in murine melanoma. (2020) (4)
- A Family with an Inverted Tandem Duplication 5q22.1q23.2 (2012) (4)
- Three new cases with a supernumerary ring chromosome 1 (2005) (4)
- First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations (2020) (4)
- Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro study. (2014) (4)
- Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus (2016) (4)
- Evolution of the parthenogenetic rock lizard hybrid karyotype: Robertsonian translocation between two maternal chromosomes in Darevskia rostombekowi (2020) (4)
- Interstitial duplication of chromosome region 1q25.1q25.3: Report of a patient with mild cognitive deficits, tall stature and facial dysmorphisms (2015) (4)
- A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia. (2009) (4)
- Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation? (2010) (4)
- Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2) (2006) (4)
- Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p? (2010) (4)
- Data Preparation in Large Real-World Data Mining Projects: Methods for Imputing Missing Values (2003) (4)
- Regional localization of 10 mariner transposon-like ESTs by means of FISH—evidence for a correlation with fragile sites (2001) (4)
- Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21 (2001) (4)
- THAI SOUTHERN PIG-TAILED MACAQUE ( MACACA NEMESTRINA ) BY MULTICOLOR BANDING (2014) (4)
- Effect of Glutathione S-transferase mu 1 (GSTM1) gene polymorphism on chronic myeloid leukemia risk and Imatinib treatment response (2017) (3)
- Use of fluorescence in-situ hybridization (fish) for the estimation of the aberrant cell clone in leukemias with trisomy-8 or monosomy-7 detected by karyotyping. (1993) (3)
- A chronic myeloid leukemia case with a unique variant Philadelphia translocation : t ( 9 ; 22 ; 21 ) ( q 34 ; q 11 ; p 12 ) (2012) (3)
- A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients. (2001) (3)
- Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44) (2018) (3)
- Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines (2012) (3)
- Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization (2017) (3)
- Molecular cytogenetic pilot study on pleomorphic adenomas of salivary glands (2019) (3)
- Chapter 6 – CG-CNVs in Genetic Diagnostics and Counseling (2014) (3)
- De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report (2021) (3)
- A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. (2013) (3)
- Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines (2020) (3)
- Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13). (2010) (3)
- Cytogenomics of six human trophoblastic cell lines. (2020) (3)
- A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1: The Contribution of Molecular Approaches for Revealing t(8;21) Variants (2015) (3)
- Partial monosomy 3q26.33-3q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case report (2014) (3)
- The internet page on small supernumerary marker chromosomes (sSMC) (2009) (3)
- A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia (2011) (3)
- A 33-year-old male patient with paternal derived duplication of 14q11.2–14q22.1~22.3: clinical course, phenotypic and genotypic findings (2016) (3)
- Nucleus Extraction from Formalin Fixed/paraffin Embedded Tissue (2002) (3)
- Disruption of PCDH10 and TNRC18 Genes due to a Balanced Translocation (2020) (3)
- Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND). (2017) (3)
- Algorithm for the diagnosis of patients with neurodevelopmental disorders and suspicion of a genetic syndrome. (2020) (3)
- High Genetic Diversity despite Conserved Karyotype Organization in the Giant Trahiras from Genus Hoplias (Characiformes, Erythrinidae) (2021) (3)
- Telomere Length Measurement by FISH (2017) (3)
- Brief Gene Mapping Reports A / B / C / D / E / F / G (2002) (3)
- Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis (2003) (3)
- Highly complex karyotypic changes in acute myelogenous leukemia: a case report. (2003) (3)
- Formation of Small Supernumerary Marker Chromosomes (2012) (3)
- Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis. (2010) (3)
- Nucleus Extraction from Cryofixed Tissue (2002) (3)
- An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations (2014) (3)
- Doxorubicin-Induced Translocation of mtDNA into the Nuclear Genome of Human Lymphocytes Detected Using a Molecular-Cytogenetic Approach (2020) (3)
- De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome. (2018) (3)
- X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU) (2017) (3)
- Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progession-related mechanisms (2006) (3)
- A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17). (2010) (3)
- Erratum to “Nucleus extraction from single mounted tissue sections” (2001) (3)
- Three-Dimensional Interphase Analysis Enabled by Suspension FISH (2009) (3)
- EXPERT KNOWLEDGE ON HUMAN GENETIC COUNSELLING AND CHROMOSOMICS ARE NECESSARY FOR SOUND GENETIC LABORATORY DIAGNOSTICS (2018) (3)
- Chromosome gain and loss in paraffin sections from malignant melanomas of the skin. (1997) (3)
- Evolutionary breakpoint regions and chromosomal remodeling in Harttia (Siluriformes: Loricariidae) species diversification (2022) (3)
- High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis) (2014) (3)
- Clinical and morphological phenotype of HMSN 1A mosaicism (1997) (3)
- Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes (2014) (2)
- Identification of potential novel drug resistance mechanisms by genomic and transcriptomic profiling of colon cancer cells with p53 deletion (2021) (2)
- Classical and molecular cytogenetics of Belontia hasselti (Perciformes: Osphronemidae): Insights into the ZZ/ZW sex chromosome system (2021) (2)
- Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8 (2017) (2)
- Human ring chromosomes and small supernumerary marker chromosomes—do they have telomeres? (2012) (2)
- Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report (2017) (2)
- Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14 (2020) (2)
- Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma. (2011) (2)
- Cytogenomics Unveil Possible Transposable Elements Driving Rearrangements in Chromosomes 2 and 4 of Solea senegalensis (2021) (2)
- Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 (2021) (2)
- A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis. (2010) (2)
- A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement (2015) (2)
- Two- to Three-Color FISH (2017) (2)
- Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report. (2020) (2)
- Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH (2014) (2)
- Loci-specific RNP-rich nuclear domains on lampbrush chromosomes: data pointing at RNA editing (2018) (2)
- About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI (2021) (2)
- Expression pattern of the peripheral myelin protein 22kDa (PMP22) in neural and non-neural tissue types of adult wildtype and Trembler mice--a comparative study. (1998) (2)
- Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome. (2010) (2)
- Partial Reduction in BRCA1 Gene Dose Modulates DNA Replication Stress Level and Thereby Contributes to Sensitivity or Resistance (2022) (2)
- Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia. (2010) (2)
- Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature. (2014) (2)
- A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature (2018) (2)
- The Multicolor Fluorescence in Situ Hybridization (mFISH) Homepage (2008) (2)
- Thorough discussion of cancer research—thoughts against the main stream (2017) (2)
- Assessing Skewed X‐Chromosome Inactivation (2018) (2)
- Chromosomal Heteromorphisms and Cancer Susceptibility Revisited (2022) (2)
- Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11 (2012) (2)
- Molecular Cytogenetics: the first impact factor (2.36) (2013) (2)
- A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b). (2015) (2)
- First chromosome analysis of Thai pufferfish Pao cochinchinensis (Steindachner, 1866) (2020) (2)
- High-resolution FISH of stretched chromosome fibers (1997) (2)
- Is Molecular Cytogenetic Diagnostics of Rare Diseases in Europe Close to Extinction (2020) (2)
- Characterization of Small Supernumerary Marker Chromosomes By A Simple Molecular and Molecular Cytogenetics Approach (2007) (2)
- Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH). (2018) (2)
- Molecular Cytogenetic Characterization of an inv(Y)(p11.2q11.221∼q11.222) in a Syrian Family (2013) (2)
- Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes as in Mandrill (2017) (2)
- Cytogenetic Evolution in a Patient with Chronic developing a Secondary Acute Myelogenous Leukemia Subtype M5 Resistant to Imatinib Mesylate Therapy (2013) (2)
- FISH – the best technique in characterization of prenatally detected small supernumerary marker chromosomes (SSMC) (2016) (2)
- Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison (2021) (2)
- Broad genomic workup including optical genome mapping uncovers a DDX3X: MLLT10 gene fusion in acute myeloid leukemia (2022) (2)
- Cytogenetics and Molecular Cytogenetics (2022) (2)
- The Tage4 gene maps to rat Chromosome 1q22 (1997) (2)
- UPD Related Syndromes Caused by Imprinting (2014) (2)
- Small Supernumerary Marker Chromosomes Known To Be Correlated with Specific Syndromes (2012) (2)
- Comparative chromosomal mapping of microsatellite repeats reveals divergent patterns of accumulation in 12 Siluridae (Teleostei: Siluriformes) species (2020) (2)
- Estimation of DNA single-strand breaks by single cells gel electrophoresis in tumor cells. (1998) (2)
- Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses (2015) (2)
- An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case (2020) (2)
- Characterization of chromosomal rearrangements in pileated gibbon (Hylobates pileatus) using multiplex-FISH technique (2016) (2)
- Fluorescence In Situ Hybridization (FISH) – Quality Issues in Molecular Cytogenetics (2010) (2)
- A preliminary integrated genetic map distinguishes every chromosome pair and locates essential genes related to abiotic adaptation of Crassostrea angulata/gigas (2018) (2)
- Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array. (2011) (2)
- Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia. (2017) (2)
- Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrence using locus-specific probes and AgNOR. (2009) (2)
- Multicolor FISH in Human Cytogenetics (2006) (2)
- Acquired del(9)(p22.3) in a primary plasma cell leukemia (2013) (1)
- The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population (2006) (1)
- Tumorcytogenetic Diagnostics and Research on Uncultured Blood or Bone Marrow and Smears (2009) (1)
- Complex karyotype including ring chromosome 11 in a patient with acute myeloid leukemia: case report (2017) (1)
- Molecular Cytogenetics: the first impact factor (2.36) (2013) (1)
- Vielfarben-Fluoreszenz-in-situ-Hybridisierung (2008) (1)
- Large deletion on the Y-chromosome long arm (Yq) of C57BL/6JBomTac inbred mice (2016) (1)
- A case of aggressive medulloblastoma with multiple recurrent chromosomal alterations. (2010) (1)
- GAS6 Oncogene and Reverse MLLT3-KMT2A Duplications in an Infant with Acute Myeloid Leukemia and a Novel Complex Hyperdiploid Karyotype: Detailed High-Resolution Molecular Cytogenetic Studies (2017) (1)
- The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization (2021) (1)
- Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics (2012) (1)
- A Study on Biological Application of Ag and Co/Ag Nanoparticles Cytotoxicity and Genotoxicity (2015) (1)
- A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia. (2012) (1)
- Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia (2015) (1)
- Modern High Throughput Approaches are not meant to Replace âÂÂOldFashionedâ but Robust Techniques (2017) (1)
- Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report (2012) (1)
- Distal limb deficiency, micrognathia syndrome (OMIM 246560) and syndromic forms of split hand foot malformation (SHFM) re caused by chromosome 10q genomic rearrangements (2008) (1)
- Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case (2014) (1)
- Use of FISH analysis for prostate tumors and other tissue types. (1997) (1)
- Cytogenomic characteristics of murine breast cancer cell line JC (2021) (1)
- First classical and molecular cytogenetic analyses of Sperata acicularis (Siluriformes, Bagridae) (2021) (1)
- Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathway (2014) (1)
- Chromosomal aberrations in spontaneously aborted products of conception from Ukraine (2018) (1)
- Non-Invasive Prenatal Testing in Germany (2022) (1)
- Cytogenetic Analyses Detect Cryptic Diversity in Megaderma spasma from Malaysia (2022) (1)
- Subject Index Vol. 90, 2000 (2000) (1)
- Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency (2011) (1)
- Monitoring of gas station attendants exposure to benzene, toluene, xylene (BTX) using three-color chromosome painting (2014) (1)
- Analysis and pharmacological modulation of senescence in human epithelial stem cells (2022) (1)
- The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes (2022) (1)
- Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome (2012) (1)
- Complex Small Supernumerary Marker Chromosomes (2012) (1)
- Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma (2020) (1)
- Human Cytogenetics Case Report Yet Unreported Heteromorphic Variantin Chromosome 17 (2017) (1)
- Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics history (2018) (1)
- Karyotypes of trophoblastic cell lines (2016) (1)
- Influence of glutathione S-transferase (GSTT1 and GSTM1) gene polymorphism on imatinib failure in chronic myeloid leukemia patients (2015) (1)
- Interphase Molecular Cytogenetic Detection Rates of Chronic Lymphocytic Leukemia–Specific Aberrations Are Higher in Cultivated Cells Than in Blood or Bone Marrow Smears (2016) (1)
- Successful Management of Three Pregnancies Under Imatinib Treatment in a Chronic Myeloid Leukemia Patient: A Case Report and Review of the Literature (2017) (1)
- Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndrome (2018) (1)
- Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing (2000) (1)
- LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells (2018) (1)
- A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53 (2016) (1)
- 7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly—Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly? (2021) (1)
- Joubert syndrome: Molecular basis and treatment (2022) (1)
- Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia (2012) (1)
- Homemade Locus-Specific FISH Probes: Bacterial Artificial Chromosomes (2017) (1)
- Parental Origin Determination FISH: Pod-FISH (2009) (1)
- Trisomy 21 with a Small Supernumerary Marker Chromosome Derived from Chromosomes 13/21 and 18 (2010) (1)
- An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations (2014) (1)
- Acquired del(9)(p22.3) in a primary plasma cell leukemia (2013) (1)
- Cytogenetics of ovarian cancer technical overview. (2001) (1)
- Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes (2022) (1)
- Neocentric Small Supernumerary Marker Chromosomes by Chromosome (2012) (1)
- Chromosomal aberration leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: report of a Syrian couple and review of the literature . (2015) (1)
- Two different del(5q) clones in a patient with myelodysplastic syndrome (2011) (1)
- AG AND CO/AG NANOPARTICLES CYTOTOXICITY AND GENOTOXICITY STUDY ON HEP-2 AND BLOOD LYMPHOCYTES CELLS (2015) (1)
- Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies (2014) (1)
- Inheritance of Small Supernumerary Marker Chromosomes (2012) (1)
- Comprar Small Supernumerary Marker Chromosomes (sSMC) | Liehr, Thomas | 9783642207655 | Springer (2011) (1)
- Cytogenetic Investigations in Bornean Rhinolophoidea Revealed Cryptic Diversity in Rhinolophus sedulus Entailing Classification of Peninsular Malaysia Specimens as a New Species (2021) (1)
- Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report (2020) (1)
- Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations (2010) (1)
- Fluorescence In Situ Hybridization (FISH) on Human Chromosomes Using Photoprobe Biotin-labeled Probes (2003) (1)
- A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia (2019) (1)
- Dup(13)(q14.2-q14.3): Yet Another New Differential Diagnostic Aspect for Short Stature–like Phenotype (2005) (1)
- Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties (2015) (1)
- Heteromorphic variants of chromosome 9 (2013) (1)
- Classification of FISH Probes (2017) (1)
- Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. (2022) (1)
- Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event (2015) (1)
- A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia (2016) (1)
- Formation of UPD (2014) (1)
- An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia. (2020) (1)
- The Genetic Differentiation of Pyrrhulina (Teleostei, Characiformes) Species is Likely Influenced by Both Geographical Distribution and Chromosomal Rearrangements (2022) (1)
- Characterization of Mosaicism in Different Easy-to-Acquire Body Tissues Such As Buccal Smears, Skin Abrasions, Hair Root Cells, or Urine (2017) (1)
- X chromosome aneuploidy in the Alzheimer’s disease brain (2014) (1)
- Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. (2012) (1)
- Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. (2011) (1)
- Isochromosome 17 q in Chronic Lymphocytic Leukemia (2015) (1)
- BIRC3 as a yet underestimated prognostic marker of malignancies (2016) (1)
- Chapter 4 – Formation of CG-CNVs (2014) (1)
- Characterization of Mosaicism in Various Easy-to-Acquire Body Tissues Such as Buccal Smears, Hair Root Cells or Urine (2009) (1)
- Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report (2010) (1)
- Fluorescence in situ hybridization on G-banded chromosome preparations mounted with Eukitt in a retrospective study and in routine diagnostics. (1998) (1)
- Comparative study of four Mystus species (Bagridae, Siluriformes) from Thailand: insights into their karyotypic diversity (2021) (1)
- High-quality CGH slides irrespective of the lymphocyte suspension used (2001) (1)
- The need for recognition of core professional groups in genetics healthcare services in Europe (2022) (1)
- Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae) (2013) (1)
- New BAC probe set to narrow down chromosomal breakpoints in small and large derivative chromosomes, especially suited for mosaic conditions. (2015) (1)
- A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosis. (2014) (1)
- Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1 (1997) (1)
- First Comprehensive Characterization of Phayre’s Leaf-Monkey (Trachypithecus phayrei) Karyotype (2022) (0)
- Interphase FISH in Diagnostics (2017) (0)
- Contents Vol. 134, 2015 (2015) (0)
- First Cytogenomic Characterization of the Murine Testicular Tumor Cell Line I-10 (2022) (0)
- Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia (2014) (0)
- Reviewer acknowledgement 2013 (2013) (0)
- Partial Trisomy 1q21-qter and Partial Monosomy 7q21-qter Due to a Derivative Chromosome 7 in Myelodysplastic Syndrome Associated with Squamous Cell Carcinoma: Case Report (2016) (0)
- Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality (2014) (0)
- Genetic alterations of gliomas (2019) (0)
- Correction: Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male (2009) (0)
- Molecular Cytogenomic Characterization of Two Murine Liver Cancer Cell Lines: MH-22A and Hepa 1-6 (2021) (0)
- Segmental haplosufficiency: transmitted deletions of 2p12 have no apparent phenotypic consequences (2004) (0)
- Emerging patterns of genome organization in Notopteridae species (Teleostei, Osteoglossiformes) as revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH) (2019) (0)
- Application of FISH technique using new chromosome 12 band-specific probe in four testicular germ cell i(12p)-negative tumors (2002) (0)
- First molecular cytogenetic characterisation of tracheal squamous cell carcinoma cell line KLN 205 (2021) (0)
- Structural and Numerical Abnormalities of Chromosome 18 Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving (2013) (0)
- Contents Vol. 112, 2006 (2006) (0)
- Subtelomeric and/or Subcentromeric Probe Sets (2009) (0)
- (Cyto)genomic and epigenetic characterization of BICR 10 cell line and three new established primary human head and neck squamous cell carcinoma cultures (2019) (0)
- Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports (2017) (0)
- Rapid fluorescence in situ detection of heterologous expression in E. coli and counterstaining with diamidinophenylindol. (1995) (0)
- Subject Index Vol. 86, 1999 (1999) (0)
- Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries (2019) (0)
- A genotype-phenotype correlation of small supernumerary marker chromosomes (2007) (0)
- Fusion between HTR/8SVneo and HUVEC (2011) (0)
- Leukocyte Nucleus Reveals a Linear Order of Chromosomes Separated in Two Parental Genomes That Favors the Process of Gene Activation (2018) (0)
- Comet FISH analysis for oxidative stress induced DNA damage in colon cancer relevant genes (2006) (0)
- Reviewer acknowledgement 2014 (2014) (0)
- Diagnostic applications of fluorescence in situ hybridization. (2009) (0)
- Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytes (2016) (0)
- Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia (2015) (0)
- FISH on Insect Cells Transfected with Heterologous DNA: A Single-Cell-Directed Approach (2009) (0)
- Comparative Genomic Hybridization (CGH) and Microdissection-Based CGH (Micro-CGH) (2017) (0)
- Brief Gene Mapping Reports A / B (2003) (0)
- Contents Vol. 121, 2008 (2008) (0)
- Importance of Databases for Human Genetic Diagnostics (2018) (0)
- Abstracts from the 3rd Conference on Aneuploidy and Cancer: Clinical and Experimental Aspects (2017) (0)
- Complex small supernumerary marker chromosomes – an update (2013) (0)
- Mucopolysaccharidosis type III (subtype IIIB) diagnosis as a spectrum disorder: A case report from Kosovo. (2023) (0)
- FISH on Blood or Bone Marrow Smears (2002) (0)
- Expression of the peripheral myelin protein 22 (PMP-22) during myelin development in two weeks old mice (1994) (0)
- The peripheral myelin protein 22kDa gene is expressed in non-neuronal epithelial tissues of mouse, rat, cattle and human (1997) (0)
- Correction to: The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization (2021) (0)
- Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 (2021) (0)
- Data Matching and Data Mining with EX■A■MINE: putting TRI*M results into immediate action (2004) (0)
- cenM-FISH Approaches (2009) (0)
- Prenatal diagnosis of a de novo small supernumerary marker chromosome 16 (2006) (0)
- 16p11.2-p21.2 duplication syndrome differentiated from euchromatic variation of 16p11.2 in three new families (2012) (0)
- Resource Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish Graphical (2015) (0)
- Gene expression profiling of multidrug resistant cem/adr-5000 and sensitive ccrf-cem leukemia cells to shed light on drug resistance mechanisms of tumors (2015) (0)
- 11p13 Deletion Syndrome: First Case in Morocco Detected by FISH (2014) (0)
- Reviewer acknowledgement 2015 (2015) (0)
- IDENTIFICATION OF CYTOGENETICALLY VISIBLE mtDNA IN INTERPHASE NUCLEI OF HUMAN BLOOD LYMPHOCYTES EXPOSED TO DOXORUBICIN (2020) (0)
- Tracking the evolutionary pathway of sex chromosomes among fishes: characterizing the unique XX/XY1Y2 system in Hoplias malabaricus (Teleostei, Characiformes) (2017) (0)
- Segregation analysis of paracentric inversions in human sperm: inverted segment size, low copy repeats (LCRs) and recombination hot spots have a story to tell (2008) (0)
- Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex (2016) (0)
- Comparative Molecular Cytogenetics and Chromosome Evolution (2004) (0)
- (Cyto)genomic and epigenetic characterization of BICR 10 cell line and three new established primary human head and neck squamous cell carcinoma cultures (2019) (0)
- Bar Coding Is Back (2017) (0)
- UPD of Unclear Parental Origin by Chromosome (2014) (0)
- Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to Chromosome 6q16–23 by means of FISH (1996) (0)
- Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes (2022) (0)
- Multipoint genetic linkage analysis of the m2 human muscarinic receptor gene (1995) (0)
- Contents Vol. 114, 2006 (2006) (0)
- Tumorcytogenetic Diagnostics and Research on Blood and Bone Marrow Smears or Effusions (2017) (0)
- COMPARATIVE IN VITRO STUDY OF AG AND CO/AG NANOPARTICLES MEDIATED BY PHOTOTHERMAL THERAPY OF CANCER (2015) (0)
- Contents Vol. 114, 2006 (2006) (0)
- FISH in Uncultivated Amniocytes (2017) (0)
- Molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 11 in a mother and a child with distinct phenotypes (2008) (0)
- Subject Index Vol. 91, 2000 (2000) (0)
- 3D genome topologies distinguish pluripotent epiblast and primitive endoderm cells in the mouse blastocyst (2022) (0)
- A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome (2017) (0)
- A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case (2013) (0)
- Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensis (2016) (0)
- Contents Vol. 126, 2009 (2010) (0)
- KMT2A-MLLT1 and the Novel SEC16A-KMT2A in a Cryptic 3-Way Translocation t(9;11;19) Present in an Infant With Acute Lymphoblastic Leukemia (2021) (0)
- Commercial FISH Probes (2017) (0)
- Microwave Treatment for Better FISH Results in a Shorter Time (2017) (0)
- False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests? (2022) (0)
- Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability (2022) (0)
- sSMC Characterization in a Male with Turner Syndrome Stigmata (2018) (0)
- Chromosomes of Asian Cyprinid Fishes: Genomic Differences in Conserved Karyotypes of ‘Poropuntiinae’ (Teleostei, Cyprinidae) (2023) (0)
- First cytogenomic characterization of murine testis tumor cell line MLTC-1 (2022) (0)
- Subject Index Vol. 1, 2007 (2008) (0)
- Genomic instability in the schizophrenia brain: Highlighting new intracellular mechanism for pathopsychophysiology of brain diseases (2008) (0)
- Reviewer acknowledgement 2015 (2015) (0)
- Application of FISH to Previously GTG-Banded and/or Embedded Cytogenetic Slides (2017) (0)
- Aneuploidy-driven non-heritable genomic variations demonstrate area-specific distribution in the Alzheimer’s disease brain (2013) (0)
- Invited Lectures (2009) (0)
- Prenatal ultrasonographic manifestations of partial trisomy (2020) (0)
- Contents Vol. 1, 2007 (2008) (0)
- Supernumerary Marker of Chromosome 15 Associated with Paternal Uniparental Disomy in a Case with Angelman Syndrome (2019) (0)
- 53. Multidimensional cytogenetics workup on a rare chromosomal aberration (2018) (0)
- Contents Vol. 136, 2012 (2012) (0)
- Evolution of ancient satellite DNAs in extant alligators and caimans (Crocodylia, Reptilia) (2023) (0)
- Interphase cytogenetics in paraffin-embedded ovarian tissue. (2001) (0)
- banding and region specific FISH probes characterised by high resolution multicolour Chromosome 2 aberrations in clinical cases (2005) (0)
- FISH on Insect Cells Transfected with Heterologous DNA (2002) (0)
- 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature (2016) (0)
- MOLECULAR CYTOGENETIC STUDIES IDENTIFY NOVEL CHROMOSOMAL ABERRATIONS IN MYELOID MALIGNANCES OF FANCONI ANEMIA (2016) (0)
- Supplementary Material for: Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome (2017) (0)
- Heterochromatin-Directed mFISH (HCM-FISH) (2017) (0)
- Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population (2020) (0)
- Low grade mosaicism in marker chromosomes (2009) (0)
- The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system (2022) (0)
- Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes (2019) (0)
- UPD of Multiple Chromosomes or Chromosomal Regions (2014) (0)
- Chromosome Architecture Studied by High-Resolution FISH Banding in Three Dimensionally Preserved Human Interphase Nuclei (2013) (0)
- Brief Gene Mapping Reports A / B / C (2003) (0)
- Parental origin of deletions and duplications – about the necessity to check for cryptic inversions (2018) (0)
- Multicolour FISH versus array CGH techniques. Which to choose for the characterization of small supernumerary marker chromosomes (2009) (0)
- A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7. (2013) (0)
- First report on a 20qh+ heteromorphism characterized by molecular cytogenetics as amplification of D20Z1 sequences (2019) (0)
- Prikaz de novo slučaja mozaičnog marker kromosoma 5p (2018) (0)
- Regional localization of Flic1, a calcyclin/S100A6-like gene, to rat Chromosome 7q22-31 by means of FISH (2009) (0)
- Comparative cytogenomic analysis of Cardinal fishes (Perciformes, Apogonidae) from Thailand (2021) (0)
- A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome (2020) (0)
- First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease (2016) (0)
- Reviewer acknowledgement 2016 (2016) (0)
- The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases (2021) (0)
- Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell lines (2018) (0)
- Front & Back Matter (2012) (0)
- Comparative cytogenetics in the genus Hoplias (Characiformes, Erythrinidae) highlights contrasting karyotype evolution among congeneric species (2015) (0)
- Preface (2006) (0)
- Reviewer acknowledgement 2014 (2014) (0)
- Maternal UPD by Chromosome (2014) (0)
- Integrated gene mapping and synteny studies give insights into the evolution of a sexual proto-chromosome in solea senegalensis: testing innovative molecular cytogenetic approaches for basic and diagnostic research (2015) (0)
- Parental origin of multiple small supernumerary marker chromosomes: evidence from a rare prenatal and postnatal case (2015) (0)
- Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting (2016) (0)
- Mapping of two different alpha-l,2-fucosyltransferase genes to rat Chromosome 1q22–q31 (1997) (0)
- Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment (2015) (0)
- Towards a genotype-phenotype correlation of cases with small supernumerary marker chromosomes. (2006) (0)
- High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia (2015) (0)
- Partial Trisomy 1 q 21-qter and Partial Monosomy 7 q 21-qter Due to a Derivative Chromosome 7 in Myelodysplastic Syndrome Associated with Squamous Cell Carcinoma : Case Report (2016) (0)
- Influence of aflatoxin B1 on copy number variants in human leukocytes in vitro (2015) (0)
- The meiotic segregation of paracentric inversions: how breakpoint mapping can make the difference (2008) (0)
- Reviewer acknowledgement 2016 (2016) (0)
- Chromosome Architecture Studied by High-Resolution FISH Banding in Three-Dimensionally Preserved Human Interphase Nuclei (2020) (0)
- Short communication Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia (2010) (0)
- Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation? (2019) (0)
- Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines (2020) (0)
- Molecular cytogenetics (2021) (0)
- Contents Vol. 151, 2017 (2017) (0)
- Prenatal detection of cryptic genomic rearrangement: role of detailed family history, pedigree analysis and advanced genomic technologies (2017) (0)
- CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes (2016) (0)
- Draft Spatial organization of fibroblast and spermatocyte nuclei with different B chromosome content in Korean field mouse Apodemus peninsulae (2017) (0)
- Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation (2015) (0)
- Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus (2016) (0)
- Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing (2016) (0)
- “Classical cytogenetics” is not equal to “banding cytogenetics” (2017) (0)
- O▪84 The importance of a full chromosome count (2005) (0)
- Cytogenetics (1982) (0)
- A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) (2020) (0)
- Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants (2016) (0)
- CG-CNVs: What Is the Norm? (2014) (0)
- The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases (2021) (0)
- FISH on Uncultured Blood or Bone Marrow (2002) (0)
- User-Friendly Approach to Gain Isolation of Interphase Cells for Fluorescence in Situ Hybridization (2018) (0)
- Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia‐related changes (2022) (0)
- Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species (2018) (0)
- Analysis of copy number variations induced by ultrashort electron beam radiation in human leukocytes in vitro (2019) (0)
- About the origin of the acrocentric part of non-acrocentric satellited chromosomes in humans (2021) (0)
- Imbalances of distal 8p: extent, parental origin, predisposition and clinical significance (2004) (0)
- Functional Characterization of Transgenic Mice Overexpressing Human 15-Lipoxygenase-1 (ALOX15) under the Control of the aP2 Promoter (2023) (0)
- First molecular cytogenetic characterization of the MMT 060562 murine breast cancer cell line (2021) (0)
- Bibliography of Ulrich Wolf (2001) (0)
- Revisiting the Karyotype Evolution of Neotropical Boid Snakes: A Puzzle Mediated by Chromosomal Fissions (2020) (0)
- Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes (2021) (0)
- Small supernumerary marker chromosome derived from chromosome 5-genotype phenotype correlation of proximal chromosome 5 imbalances (2011) (0)
- Molecular Cytogenetic Characterization of the Murine Melanoma Cell Lines S91 Clone M3 and B16-F1 with Variant B16-4A5 (2021) (0)
- A De Novo Childhood Case of T-cell Lymphoblastic Leukemia with High Hyperdiploid Karyotype Carrying an Unreported Balanced Translocation t(X;5)(q26;q31.3~32) in A Male Patient (2018) (0)
- Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family (2022) (0)
- Cytogenomics of murine melanoma cell lines C57/B1 and B16-F0 (2020) (0)
- Contents Vol. 90, 2000 (2000) (0)
- About Cryptic Acrocentric Pericentromeric Abnormalities in Infertile (2021) (0)
- Detection oftheCMTlA/HNPPrecombination hotspot inunrelated patients ofEuropean (1997) (0)
- Micro-CGH: Microdissection-Based Comparative Genomic Hybridization (2009) (0)
- Mosaicism in the human brain. Possible diagnostic relevance in molecular cytogenetics of the future (2014) (0)
- Heterochromatic regions in Japanese quail chromosomes: comprehensive molecular-cytogenetic characterization and 3D mapping in interphase nucleus (2018) (0)
- Molecular cytogenetic characterization of the urethane-induced murine lung cell line LA-4 as a model for human squamous cell lung cancer (2021) (0)
- Measuring Telomere Length: A Timeline Review on the State-of-Art Techniques (2021) (0)
- Expression of peripheral myelin protein-22 (PMP22)-mRNA in hereditary motor and sensory neuropathy type 1 (HMSN 1) (1997) (0)
- Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH) (2014) (0)
- Complex karyotype involving six chromosomes, with one dicentric and three yet unreported acquired chromosomal aberrations in a case of splenic marginal zone lymphoma (2017) (0)
- Cytogenetic mechanisms of unisexuality in rock lizards (2020) (0)
- Small Supernumerary Marker Chromosomes in Genetic Diagnostics and Counseling (2012) (0)
- Correction: Chromosomal Mapping of Repetitive DNAs in Triportheus trifurcatus (Characidae, Characiformes): Insights into the Differentiation of the Z and W Chromosomes (2014) (0)
- Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species (2017) (0)
- A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome (2020) (0)
- Uniparental disomy is a chromosomic disorder in the first place (2022) (0)
- Molecular combing and its application in clinical settings (2022) (0)
- Cytogenomic characteristics of murine breast cancer cell line JC (2021) (0)
- CENP Antibodies Used Additionally to FISH (2017) (0)
- Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia (2020) (0)
- Chromosomes in a genome-wise order: evidence for metaphase architecture (2016) (0)
- Molecular karyotyping (2021) (0)
- Centric Small Supernumerary Marker Chromosomes (2012) (0)
- Small Supernumerary Marker Chromosomes Additionally to Other Chromosomal Rearrangements (2012) (0)
- Patient Organizations in Connection with UPD (2014) (0)
- Contents Vol. 91, 2000 (2001) (0)
- Contents Vol. 128, 2010 (2010) (0)
- Chapter 7 – Online Resources (2014) (0)
- FISH and Chips on the Internet (2009) (0)
- Aneuploidy-driven non-heritable genomic variations demonstrate area-specific distribution in the Alzheimer’s disease brain (2013) (0)
- First report on a 20 qh + heteromorphism characterized by molecular cytogenetics as amplification of D 20 Z 1 sequences (0)
- Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds (2022) (0)
- Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis (2018) (0)
- Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report (2022) (0)
- A Case with Double Translocation and Sjögren's Syndrome (2013) (0)
- Unreported combination of rearrangements in a childhood B-cell acute lymphoblastic leukemia case: Coexistence of translocation t(8;14) and monoallelic loss of tumor suppressor gene TP53 (2018) (0)
- How to Obtain High‐Quality Metaphase Spreads for Molecular Cytogenetics (2022) (0)
- ISCN (2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis (2009) (0)
- Short communication A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia (2009) (0)
- O9: Array CGH using microdissected chromosomes to map chromosomal breakpoints (2005) (0)
- Subject Index Vol. 93, 2001 (2001) (0)
- First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae) (2013) (0)
- Cryptic NUP214-ABL1 fusion with complex karyotype, episomes and intra-tumor genetic heterogeneity in a T-cell lymphoblastic lymphoma (2018) (0)
- Molecular cytogenetic characterization of four new cases with a small supernumerary marker chromosome derived from chromosome 16 (2009) (0)
- Multiphoton multicolor FISH (2000) (0)
- Contents Vol. 139, 2013 (2013) (0)
- About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI (2021) (0)
- Next‐generation phenotyping in cat‐eye syndrome based on computer‐aided facial dysmorphology analysis of normal photographs (2021) (0)
- A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) (2020) (0)
- Multi‐color FISH assays for characterization of marker chromosomes and epigenetic changes (2009) (0)
- Genomic Organization of Microsatellites and LINE-1-like Retrotransposons: Evolutionary Implications for Ctenomys minutus (Rodentia: Ctenomyidae) Cytotypes (2022) (0)
- MOLECULAR CYTOGENETIC CHARACTERISTICS OF 24 VARIANT PHILADELPHIA TRANSLOCATIONS IN SYRIAN CHRONIC MYELOID LEUKEMIA PATIENTS: A CLOSER LOOK ON THE DERIVATIVE CHROMOSOMES 9 (2015) (0)
- Preface (2021) (0)
- Abstracts from the 3rd Conference on Aneuploidy and Cancer: Clinical and Experimental Aspects (2017) (0)
- Chromosomes of Asian cyprinid fishes: cytogenetic analysis of two representatives of small paleotetraploid tribe Probarbini (2018) (0)
- Small supernumerary marker chromosomes – an update (2014) (0)
- Chapter 5 – Types of CG-CNVs (2014) (0)
- Evaluation of chromosomal mosaicism by aCGH and MLPA:molecular characterization of mosaic ring chromosome 22. (2013) (0)
- Myelodysplastic syndrome without ring sideroblasts and with Janus kinase 2 gene mutation: An unusual case report. (2016) (0)
- Chapter 3 – Inheritance of CG-CNVs (2014) (0)
- Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter) (2020) (0)
- 14th Workshop on Fetal Cells and Fetal DNA (2005) (0)
- De novo translocation involving two chromosomes in adult prolymphocytic leukemia--a rare case. (2010) (0)
- Contents Vol. 142, 2014 (2014) (0)
- The analysis of chromosomal instability in 18 tumor patients with strong acute and/or late side effects by G2-aberration assay and/or whole chromosome painting (2001) (0)
- FISH on Hair Root Cells (2002) (0)
- Preface to the First Edition (2002) (0)
- Distribution of radiation-induced chromosomal aberrations in a NBS-family A M-FISH study (2001) (0)
- Ataxia-telangiectasia paradoxes: spotlight on post-zygotic chromosome instability in the brain and its contribution to neurodegeneration pathways (2013) (0)
- Characterization of chromosomal rearrangements in pileated gibbon (Hylobates pileatus) using multiplex-FISH technique (2016) (0)
- Editor's Note: Journal of Genetics and Genomes (2017) (0)
- Ataxia-telangiectasia paradoxes: spotlight on post-zygotic chromosome instability in the brain and its contribution to neurodegeneration pathways (2013) (0)
- Application of FISH to Archival Cytogenetic Slides (2009) (0)
- A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome – evidence for an underestimated entity? (2010) (0)
- Progress in molecular diagnosis of Charcot-Marie-Tooth-disease type 1 (CMT 1, HMSN I) and hereditary neuropathy with liability to pressure palsies (HNPP) by fluorescence in situ hybridization (FISH)-detection of a potential genetic mosaicism (1994) (0)
- Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome (2022) (0)
- Comparative cytogenomic analysis of Cardinal fishes (Perciformes, Apogonidae) from Thailand (2021) (0)
- Complex chromosomal rearrangements in peripheral blood and decreased amount of natural killer cells in two female gas station attendants of Rio de Janeiro (2015) (0)
- First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations (2020) (0)
- Thymocyte Development CD8 Locus Nuclear Dynamics during (2010) (0)
- Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes (2014) (0)
- Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44) (2018) (0)
- The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes (2022) (0)
- Detailed characterization of small supernumerary marker chromosomes reveals breakpoint hot spots and narrows down the critical regions of clinical impact. (2010) (0)
- UPD in Diagnostics and Genetic Counseling (2014) (0)
- Murine multicolor banding. (2013) (0)
- Interphase cytogenetics in frozen ovarian tumor tissue. (2001) (0)
- FISH—Banding Methods and Clinical Applications (2004) (0)
- Giant Sex Chromosomes in Omophoita Species (Coleoptera, Chrysomelidae): Structural and Evolutionary Relationships Revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH) (2023) (0)
- Characterization of RB1 Deletions in Interphase and Metaphase by Molecular Cytogenetics Exemplified in Chronic Lymphatic Leukemia. (2018) (0)
- A New Case of Childhood Acute Lymphoblastic B-Cell Leukemia from Pristina (2023) (0)
- Abstract 254: A HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis (2010) (0)
- Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell lines (2018) (0)
- Contents Vol. 93, 2001 (2001) (0)
- Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event (2015) (0)
- Nuclear architecture (2021) (0)
- P4 A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues (2010) (0)
- An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case (2020) (0)
- Werner Schmid, 1930–2002 (2002) (0)
- Integrating Cytogenetics and Population Genomics: Allopatry and Neo-Sex Chromosomes May Have Shaped the Genetic Divergence in the Erythrinus erythrinus Species Complex (Teleostei, Characiformes) (2022) (0)
- MLLT 10 and IL 3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia : A case report (2014) (0)
- PB1662 INTEGRATION OF GENOME-WIDE ANALYSIS INTO CLINICAL DIAGNOSIS OF ACUTE LYMPHOBLASTIC LEUKEMIA: HOW MUCH CAN WE IMPROVE CYTOGENETIC TESTING? (2019) (0)
- Constitutional Partial Proximal Trisomy 14q11.2 to 14q21: Two New Moroccan Cases and Review of the Literature (2018) (0)
- Evolutionary tracks of chromosomal diversification in Trichopsis (Anabantiformes, Osphronemidae) fishes: New insights from a molecular cytogenetic perspective (2023) (0)
- Multiple Small Supernumerary Marker Chromosomes (2012) (0)
- Reviewer acknowledgement 2013 (2013) (0)
- Balanced X autosome translocation suggests association of AMMECR1 disruption with hearing loss short stature bone and heart alterations (2017) (0)
- How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set (2012) (0)
- C-type lectins and human epithelial membrane protein1: Are they new proteins in keratin disorders? (2013) (0)
- A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome (2020) (0)
- A preliminary integrated genetic map distinguishes every chromosome pair and locates essential genes related to abiotic adaptation of Crassostrea angulata/gigas (2018) (0)
- Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report (2020) (0)
- Targeted Treatment and Immunotherapy in High-risk and Relapsed/Refractory Pediatric Acute Lymphoblastic Leukemia (2022) (0)
- Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH (2014) (0)
- Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes (2021) (0)
- Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma. (2013) (0)
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