Thomas Liehr

Thomas Liehr's AcademicInfluence.com Rankings

Thomas Liehr

Biology

#8680

World Rank

#11796

Historical Rank

Cell Biology

#350

World Rank

#359

Historical Rank

Genetics

#871

World Rank

#966

Historical Rank

Molecular Biology

#1124

World Rank

#1149

Historical Rank

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Biology

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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 Ã¢ÂÂOldFashionedÃ¢ÂÂ 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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Thomas Liehr is affiliated with the following schools:

Yerevan State University
University of Jena
Yerevan State Medical University

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