Felix Mitelman

Q: What Schools Are Affiliated With Felix Mitelman

Felix Mitelman is affiliated with the following schools: Leiden University, University of Southern Denmark, University of California, Berkeley, California Institute of Technology, Stanford University, Lund University

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Felix Mitelman

Physics

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#3716

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Physics

Felix Mitelman's Degrees

Bachelors Physics University of California, Berkeley
PhD Physics Stanford University

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Felix Mitelman'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

Catalogue of chromosome aberrations in cancer. (1983) (1515)
The impact of translocations and gene fusions on cancer causation (2007) (1272)
ISCN 1995 : an international system for human cytogenetic nomenclature (1995) : recommendations of the International Standing Committee on Human Cytogenetic Nomenclature : Memphis, Tennessee, USA, October 9-13, 1994 (1995) (817)
The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein (1996) (743)
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia (1997) (707)
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. (1994) (530)
ISCN 1991 : guidelines for cancer cytogenetics : supplement to An international system for human cytogenetic nomenclature : recommendations of the Standing Committee on Human Cytogenetic Nomenclature, Subcommittee on Cancer Cytogenetics (1992) (507)
The emerging complexity of gene fusions in cancer (2015) (487)
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. (1997) (469)
Mitelman database of chromosome aberrations and gene fusions in cancer (2014) (452)
Cytogenetic and Molecular Genetic Evolution of Chronic Myeloid Leukemia (2002) (431)
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors (2001) (431)
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. (2000) (407)
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. (1996) (341)
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer (2004) (333)
Recurrent chromosome aberrations in cancer. (2000) (326)
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11) (1992) (304)
Fusion of the EWS and CHOP genes in myxoid liposarcoma. (1996) (293)
Chromosomes and cancer. (2009) (290)
Clustering of aberrations to specific chromosomes in human neoplasms. IV. A survey of 1,871 cases. (2009) (276)
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976–1993 and on 5098 unselected cases reported in the literature 1974–2001 (2002) (265)
Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia. (1981) (237)
Clustering of aberrations to specific chromosomes in human neoplasms. (2009) (237)
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13). (2001) (207)
Clustering of aberrations to specific chromosomes in human neoplasms. III. Incidence and geographic distribution of chromosome aberrations in 856 cases. (2009) (207)
Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups (1995) (205)
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity. (2005) (192)
The cytogenetic scenario of chronic myeloid leukemia. (1993) (191)
Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor Loci (1993) (190)
Isochromosomes in neoplasia (1994) (189)
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group). (1996) (188)
Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia (1978) (188)
Cytogenetic analysis of 57 primary prostatic adenocarcinomas (1992) (184)
Primary vs. secondary neoplasia‐associated chromosomal abnormalities—balanced rearrangements vs. genomic imbalances? (1996) (182)
Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia (2016) (182)
Trisomy 7 in nonneoplastic cells (1993) (178)
Report of the committee on chromosome and gene loss in human neoplasia (1991) (174)
Cytogenetic analysis of 363 consecutively ascertained diffuse large B‐cell lymphomas (1999) (171)
Cytogenetic evolution patterns in non-Hodgkin's lymphoma. (1995) (170)
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: A report of the CHAMP study group (1998) (169)
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. (1996) (163)
Report of the committee on chromosome changes in neoplasia (1990) (160)
A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas. (1988) (156)
Tumor Etiology and Chromosome Pattern (1972) (151)
Genetic convergence and divergence in tumor progression. (1988) (149)
Trisomy 7 and sex chromosome loss in human brain tissue. (1989) (147)
Report of the committee on structural chromosome changes in neoplasia. (1988) (147)
Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern. (1993) (143)
Non‐random karyotypic evolution in chronic myeloid leukemia (1976) (141)
Clinical significance of cytogenetic findings in solid tumors. (1997) (140)
Chromosome analysis of 96 uterine leiomyomas. (1991) (138)
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas (2004) (136)
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution (2004) (136)
Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue. (1990) (135)
Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors (1994) (132)
Immune‐mediated complications in patients with myelodysplastic syndromes – clinical and cytogenetic features (1995) (131)
The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats. (2004) (130)
Chromosomal abnormalities and their clinical significance in acute lymphoblastic leukemia. Third International Workshop on Chromosomes in Leukemia. (1983) (130)
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22) (1994) (130)
Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck (1995) (128)
Report of the committee on chromosome changes in neoplasia. (1990) (128)
Chromosome abnormalities in the myelodysplastic syndromes. (1986) (126)
Cancer cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells (2015) (126)
Quantitative acute leukemia cytogenetics (1992) (125)
Report of the committee on structural chromosome changes in neoplasia. (1989) (124)
Cytogenetic analysis of pancreatic carcinomas: Intratumor heterogeneity and nonrandom pattern of chromosome aberrations (1998) (122)
Identification by fluorescence of the G chromosome lost in human meningomas. (2009) (121)
Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma (1989) (120)
Rings, dicentrics, and telomeric association in histiocytomas. (1988) (118)
Cytogenetics of Synovial Sarcoma: Presentation of Ten New Cases and Review of the Literature (1991) (118)
Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. (1999) (117)
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. (1999) (117)
A collaborative study of the relationship of the morphological type of acute nonlymphocytic leukemia with patient age and karyotype. (1982) (115)
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells (1999) (115)
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group (2002) (114)
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations. (2005) (114)
Characterization of the 12q13-15 amplicon in soft tissue tumors. (1995) (113)
Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2. (1996) (113)
Long‐term survival of patients with acute myeloid leukemia (1997) (111)
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features (1997) (110)
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations. (1999) (110)
The 11q;22q translocation: A European collaborative analysis of 43 cases (2004) (109)
Clinical-cytogenetic correlations in myelodysplasia (preleukemia). (1989) (108)
Secondary chromosomal abnormalities in acute leukemias. (1994) (106)
Cytogenetic-Morphologic Correlations in Aneurysmal Bone Cyst, Giant Cell Tumor of Bone and Combined Lesions. A Report from the CHAMP Study Group (2000) (106)
Cytogenetic, Clinical, and Morphologic Correlations in 78 Cases of Fibromatosis: A Report from the CHAMP Study Group (2000) (105)
Whole‐arm t(1;16) and i(1q) as sole anomalies identify gain of 1 q as a primary chromosomal abnormality in breast cancer (1992) (105)
Fusion of the BCR and the fibroblast growth factor receptor‐1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: The first fusion gene involving BCR but not ABL (2001) (104)
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs: a report from an ongoing study by the European Study Group on Cytogenetic Biomarkers and Health. (1998) (103)
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution (2001) (103)
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group). (1996) (101)
Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck. (1995) (101)
An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage. (1990) (98)
CARDIAC PUNCTURE OF FETUS WITH HURLER'S DISEASE AVOIDING ABORTION OF UNAFFECTED CO-TWIN (1978) (98)
Restricted number of chromosomal regions implicated in aetiology of human cancer and leukaemia (1984) (98)
Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy. (1992) (97)
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation. (1994) (97)
BCR/ABL‐negative chronic myeloid leukemia with ETV6/ABL fusion (1997) (96)
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature. (1991) (96)
Chromosomal rearrangements in chondromatous tumors (1990) (95)
Reciprocal translocation t(3;12)(q27;q13) in lipoma. (1986) (94)
Lipomas have characteristic structural chromosomal rearrangements of 12q13‐q14 (1987) (94)
MDM2 gene amplification correlates with ring chromosomes in soft tissue tumors (1994) (94)
Numerical chromosome aberrations in human neoplasia. (1986) (93)
Nonrandom chromosomal rearrangements in pancreatic carcinomas (1992) (93)
A novel gene, MSI2, encoding a putative RNA-binding protein is recurrently rearranged at disease progression of chronic myeloid leukemia and forms a fusion gene with HOXA9 as a result of the cryptic t(7;17)(p15;q23). (2002) (92)
Chromosome aberrations and micronuclei in bone marrow cells and peripheral blood lymphocytes in humans exposed to ethylene oxide. (2008) (92)
Cytogenetic analysis in the diagnosis of acute leukemia (1992) (92)
Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate. (1988) (92)
Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas (1988) (91)
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes (2016) (90)
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. (2000) (89)
Chromosome aberrations in 35 primary ovarian carcinomas (1992) (88)
Marker ring chromosome--a new cytogenetic abnormality characterizing lipogenic tumors? (1987) (88)
The chromosomes of fifty primary Rous rat sarcomas. (2009) (87)
Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias (2000) (86)
Clustering of aberrations to specific chromosomes in human neoplasms. II. A survey of 287 neoplasms. (2009) (86)
Clonal heterogeneity in breast cancer: Karyotypic comparisons of multiple intra—and extra—tumorous samples from 3 patients (1995) (86)
Chromosome analysis of 20 breast carcinomas: Cytogenetic multiclonality and karyotypic‐pathologic correlations (1993) (85)
Cytogenetic intratumor heterogeneity in soft tissue tumors. (1994) (85)
Karyotypic abnormalities in tumours of the pancreas. (1993) (84)
Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies. (1985) (84)
A Nordic data base on somatic chromosome damage in humans. Nordic Study Group on the Health Risk of Chromosome Damage. (1990) (84)
Cytogenetic findings in 33 osteosarcomas (1993) (84)
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. (1997) (83)
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma. (2001) (83)
Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue (1993) (83)
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization (1998) (82)
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations (2005) (81)
Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas. (1993) (81)
Supernumerary ring chromosome as the sole cytogenetic abnormality in a dermatofibrosarcoma protuberans. (1990) (80)
Cytogenetic evidence for splenic origin of blastic transformation in chronic myeloid leukaemia. (2009) (80)
Non‐random chromosome changes in acute myeloid leukemia. Chromosome banding examination of 30 cases at diagnosis (1976) (80)
Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features (1993) (80)
Chromosome banding pattern in human colonic polyps. (2009) (79)
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders (2005) (79)
Cytogenetic analysis of 52 colorectal carcinomas‐‐non‐random aberration pattern and correlation with pathologic parameters (1993) (78)
Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer (1998) (77)
Secondary chromosome aberrations in the acute leukemias. (1986) (77)
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia (1987) (76)
Cytogenetic findings in malignant peripheral nerve sheath tumors (1995) (75)
Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors (1995) (74)
Reciprocal 8;14 translocation in EBV‐negative B‐cell acute lymphocytic leukemia with burkitt‐type cells (1979) (73)
Occupational exposure to petroleum products in men with acute non-lymphocytic leukaemia. (1978) (73)
FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q (1998) (73)
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis (2010) (73)
Aberrations of chromosome segment 12q13–15 characterize a subgroup of hemangiopericytomas (1993) (72)
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses (1994) (71)
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13) (2003) (70)
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42 (2006) (70)
Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP Study Group (2000) (69)
A single‐center population‐based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender (1999) (69)
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age‐ and sex‐related differences (2003) (68)
Coping with complexity. multivariate analysis of tumor karyotypes. (2002) (68)
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. (1996) (67)
Primary chromosome abnormalities in human neoplasia. (1989) (67)
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies. (2004) (67)
Trisomy 21 in neoplastic cells. (2005) (67)
Karyotypic characterization of urinary bladder transitional cell carcinomas (2000) (66)
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia (2004) (66)
Multiple apparently unrelated clonal chromosome abnormalities in a squamous cell carcinoma of the tongue. (1988) (66)
The chromosomes of primary 7,12-dimethylbenz(a)anthracene-induced rat sarcomas. (2009) (65)
Karyotypic rearrangements in 20 uterine leiomyomas. (1988) (65)
Variant Ph translocations in chronic myeloid leukemia. (1985) (65)
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p. (2000) (65)
Hibernomas are characterized by rearrangements of chromosome bands 11q13‐21 (1994) (65)
Cytogenetic monoclonality in multifocal uroepithelial carcinomas: evidence of intraluminal tumour seeding (1999) (64)
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group (2000) (64)
Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma. (1987) (63)
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA‐FISH (2001) (63)
Statistical behavior of complex cancer karyotypes (2005) (63)
Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia (1997) (63)
Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck (1990) (62)
Clinical implications of monosomy 7 in acute nonlymphocytic leukemia (1980) (62)
Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia. (1978) (61)
Chromosomal, morphological and clinical correlations in blastic crisis of chronic myeloid leukaemia: a study of 69 cases. (2009) (61)
Bone marrow karyotype and prognosis in primary myelodysplastic syndromes (1988) (61)
Deletion of chromosome arm 3p in hematologic malignancies (1997) (60)
Trisomy 12 in uterine leiomyomas. A new cytogenetic subgroup. (1990) (60)
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1‐13.2 (1998) (60)
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition. (2002) (60)
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology. (2001) (60)
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia. (2003) (60)
Cytogenetically unrelated clones in hematological neoplasms. (1989) (60)
Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas (1989) (59)
International standing committee on human cytogenetic nomenclature (1996) (59)
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients (2004) (59)
The specificity of chromosome A2 involvement in DMBA-induced rat sarcomas. (2009) (59)
Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors (1990) (59)
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. (2000) (59)
Cytogenetic analysis of multifocal breast carcinomas: detection of karyotypically unrelated clones as well as clonal similarities between tumour foci. (1994) (58)
Chromosomal Abnormality T(9;22)(Q22;Q12) In an Extraskeletal Myxoid Chondrosarcoma Characterized By Fine Needle Aspiration Cytology, Electron Microscopy, Immunohistochemistry and Dna Flow Cytometry (1991) (58)
Correlation between karyotypic pattern and clinicopathologic features in 125 breast cancer cases (1996) (58)
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients (1998) (57)
Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate (1990) (57)
Tumor karyotype predicts clinical outcome in colorectal cancer patients. (2004) (56)
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group. (1998) (56)
Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements. (1988) (56)
Marker chromosome 14q + in human cancer and leukemia. (1981) (55)
Clonal chromosome abnormalities in two liposarcomas. (1987) (55)
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas (1990) (55)
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias. (2010) (55)
Bilateral ovarian carcinoma: Cytogenetic evidence of unicentric origin (1991) (55)
Increased frequency of lymphocyte micronuclei in workers producing reinforced polyester resin with low exposure to styrene. (1983) (55)
CHROMOSOME ABERRATIONS AND METRONIDAZOLE (1976) (54)
Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma. (1989) (54)
Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14-15;q23-24). (1988) (53)
Ovarian carcinoma develops through multiple modes of chromosomal evolution. (2003) (53)
Chromosome rearrangements in synovial chondromatous lesions. (1996) (53)
Micronuclei and chromosome aberrations in bone marrow cells and lymphocytes of humans exposed mainly to petroleum vapors. (2009) (53)
Increased frequency of chromosome aberrations in workers exposed to styrene. (1979) (52)
Prognostic implications of chromosome analysis in acute non-lymphocytic leukemia (1977) (52)
Monoclonal origin of endometriotic cysts (1995) (52)
G-banding in Rous rat sarcomas during serial transfer: significant chromosome aberrations and incidence of stromal mitoses. (2009) (52)
Two distinct FUS breakpoint clusters in myxoid liposarcoma and acute myeloid leukemia with the translocations t(12;16) and t(16;21). (1995) (51)
Incidence of Down's syndrome in Sweden during the years 1968-1977. (1981) (51)
On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma. (1990) (51)
Interindividual variation in the responses of cultured human lymphocytes to exposure from DNA damaging chemical agents: interindividual variation to carcinogen exposure. (1978) (50)
In vivo and in vitro ethylene oxide exposure of human lymphocytes assessed by chemical stimulation of unscheduled DNA synthesis. (1981) (50)
Deletion of the short arm of chromosome 3 in breast tumors (1997) (50)
Cytogenetic analysis of 33 basal cell carcinomas. (1991) (49)
Unique balanced chromosome abnormalities in treatment‐related myelodysplastic syndromes and acute myeloid leukemia: Report from an International Workshop † (2002) (48)
Isochromosome 17 in a case of eosinophilic leukaemia. An abnormality common to eosinophilic and neutrophilic cells. (2009) (48)
Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma. (1988) (47)
High blood pressure related to carcinogen-induced unscheduled DNA synthesis, DNA carcinogen binding, and chromosomal aberrations in human lymphocytes. (1976) (47)
Isochromosomes i(8q) or i(9q) in three adenocarcinomas of the lung. (1988) (47)
Clustering of breakpoints to specific chromosomal regions in human neoplasia. A survey of 5,345 cases. (2008) (47)
Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin. (1988) (47)
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances. (2002) (47)
Characteristic karyotypic features in lacrimal and salivary gland carcinomas. (1994) (47)
Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology. (2000) (46)
Chromosomes, genes, and cancer (1994) (46)
Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma (1993) (45)
Clinical and genetic studies of ETV6/ABL1‐positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate (2003) (45)
A Short History of Chromosome Rearrangements and Gene Fusions in Cancer (2015) (45)
Poor survival in t(8;21)(q22;q22)‐associated acute myeloid leukaemia with leukocytosis (1997) (44)
Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements (1998) (44)
Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx. (1990) (44)
Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer. (1997) (44)
Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract (1991) (44)
Massive cytogenetic heterogeneity in a pancreatic carcinoma: Fifty‐four karyotypically unrelated clones (1995) (43)
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data. (2004) (43)
Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors. (1990) (43)
Characterization and chromosomal mapping of the human TFG gene involved in thyroid carcinoma. (1997) (43)
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2. (1990) (42)
Clonal chromosome aberrations in three sacral chordomas. (1994) (42)
Chromosomes and causation of human cancer and leukemia XXXV. The missing Y in acute non‐lymphocytic leukemia (ANLL) (1980) (42)
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia? (2001) (42)
Extremely long duration of chronic myeloid leukaemia with Ph1 negative and Ph1 positive bone marrow cells. (2009) (42)
Recurrent chromosome aberrations in abdominal smooth muscle tumors. (1992) (42)
Trisomy 7 in Short‐Term Cultures of Colorectal Adenocarcinomas (1991) (42)
Comparison between five Nordic laboratories on scoring of human lymphocyte chromosome aberrations. (2008) (42)
Chromosome abnormalities in cancer. (1990) (41)
Bone marrow karyotypes in 94 children with acute leukemia (1990) (41)
Correlation of Karyotype and Occupational Exposure to Potential Mutagenic/Carcinogenic Agents in Acute Nonlymphocytic Leukemia (1984) (41)
A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas (2005) (41)
Diverse chromosome abnormalities in squamous cell carcinomas of the skin. (1989) (41)
No cytogenetic effects in lymphocytes of stainless steel welders. (1983) (41)
Chromosome abnormalities are associated with unfavorable outcome in prostatic cancer patients. (1992) (40)
RT‐PCR analysis of the MOZ‐CBP and CBP‐MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13) (2000) (40)
Trisomy 2 as the sole chromosomal abnormality in a hepatoblastoma (1992) (40)
Sister chromatid exchanges and structural chromosome aberrations in relation to smoking in 91 individuals. (2008) (40)
19p + marker chromosome correlates with relapse in malignant fibrous histiocytoma (1996) (39)
Cytogenetic findings in three primary hepatocellular carcinomas. (1992) (39)
Cytogenetic studies in non-Hodgkin lymphomas--results from surgical biopsies. (2008) (39)
Different karyotypic features characterize different clinicopathologic subgroups of benign lipogenic tumors (1988) (39)
Prognostic implications of cytogenetic findings in kidney cancer. (1997) (39)
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia. (1986) (38)
New structural chromosomal rearrangements in congenital leukemia. (1987) (38)
Expression analysis and chromosomal mapping of a novel human gene, APRIL, encoding an acidic protein rich in leucines. (1998) (38)
Secondary chromosome changes in chronic myeloid leukemia: Relation to treatment (1979) (38)
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas. (1990) (38)
Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue. (1998) (38)
Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization. (1988) (37)
Cytogenetic findings in phyllodes tumors of the breast: karyotypic complexity differentiates between malignant and benign tumors. (1997) (37)
Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes. (1996) (37)
Chromosome rearrangements in two uterine sarcomas. (1990) (37)
Acute myeloid leukemia and clonal chromosome aberrations in relation to past exposure to organic solvents. (2000) (37)
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs. (1998) (37)
Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes. (1998) (36)
Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma. (1997) (36)
A simple trypsin-Giemsa technique producing simultaneous G- and C-banding in human chromosomes. (2009) (36)
Variable FHIT transcripts in non‐neoplastic tissues (1997) (36)
C-band heteromorphism in breast cancer patients. (1985) (36)
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies (2001) (36)
Cell production and cell function in human cyclic neutropenia. (2009) (35)
UNEVEN GEOGRAPHICAL DISTRIBUTION OF 15;17-TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKÆMIA (1978) (35)
Molecular screening for new fusion genes in cancer (2008) (35)
Duplication of chromosome segment 12q15‐24 is associated with atypical lipomatous tumors. A report of the CHAMP collaborative study group (1996) (35)
Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient. (1989) (35)
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynx. (1988) (35)
Geographic heterogeneity of chromosome aberrations in hematologic disorders. (1986) (35)
Prognostic implications of BCL6 rearrangement in uniformly treated patients with diffuse large B-cell lymphoma--a Nordic Lymphoma Group study. (2002) (35)
Chromosomal abnormalities in giant cell tumors of bone. (1991) (35)
Hodgkin's disease and acute leukaemia. A clinical and cytogenetic study. (2009) (35)
Double minutes in two primary adenocarcinomas of the prostate. (1989) (35)
Trisomy 7 in nonneoplastic epithelial kidney cells. (1995) (34)
Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa. (1997) (34)
Karyotypic abnormalities in fibroadenomas of the breast (1997) (34)
Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses (1995) (34)
Chromosome banding pattern in acute myeloid leukaemia. (2009) (34)
Age- and gender-related heterogeneity of cancer chromosome aberrations. (1993) (33)
Cytogenetic analysis of short-term cultured squamous cell carcinomas of the lung. (1995) (33)
Cytogenetic studies of childhood non-Hodgkin lymphomas. (2008) (33)
Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract (1992) (33)
Complex chromosome rearrangements in an extraabdominal desmoid tumor. (1988) (32)
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage‐repair mechanism in the origin of the t(8;16)(p11;p13) (2003) (32)
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia. (1993) (32)
Multicolor COBRA‐FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression (2002) (32)
Prognostic impact of chromosome aberrations in ovarian cancer. (1992) (32)
Trisomy 20 is a primary chromosome aberration in desmoid tumors (1995) (32)
Nonrandom secondary chromosome-aberrations in liposarcomas with t(12, 16). (1994) (32)
NO CYTOGENETIC EFFECT OF METRONIDAZOLE (1980) (32)
Wilms tumors develop through two distinct karyotypic pathways. (2004) (31)
Cytogenetic studies in non-Hodgkin lymphomas--results from fine-needle aspiration samples. (2008) (31)
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex (2001) (30)
No cytogenetic effects of quinolone treatment in humans (1988) (30)
Whole-exome sequencing of pediatric acute lymphoblastic leukemia (2012) (30)
Molecular analysis of simple variant translocations in acute promyelocytic leukemia (1994) (30)
Cytogenetic polyclonality in hematologic malignancies (1999) (30)
Cytogenetic analyses in 89 patients with secondary hematologic disorders--results of a cooperative study. (1987) (30)
Different patterns of chromosomal imbalances in metastasising and non‐metastasising primary breast carcinomas (1999) (30)
Evidence of somatic mutations in osteoarthritis (1996) (30)
Karyotypic characteristics of borderline malignant tumors of the ovary: trisomy 12, trisomy 7, and r(1) as nonrandom features. (1996) (29)
Chromosomal abnormalities in two bladder carcinomas with secondary squamous cell differentiation. (1998) (29)
Isolation and characterization of radiation hybrids for human chromosome 12. (1995) (29)
Trisomy 19 as the sole chromosomal anomaly in hematologic neoplasms. (1994) (29)
Micronuclei in erythropoietic bone marrow cells: relation to cytogenetic pattern and prognosis in acute nonlymphocytic leukemia. (1981) (29)
Structural chromosome aberrations in a case of angioleiomyoma. (1986) (28)
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma (1996) (28)
A gene fusion network in human neoplasia (2006) (28)
Heterogeneity of Ph1 in chronic myeloid leukaemia. (2009) (28)
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions (2021) (28)
The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14. (1989) (28)
MDS/AML‐associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q) (2004) (28)
Fluorescence in situ hybridization analysis of whole‐arm 7;12 translocations in hematologic malignancies (1995) (28)
Ring marker containing 17q and chromosome 22 in a case of dermatofibrosarcoma protuberans. (1996) (28)
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group. (2002) (28)
Cytogenetics of experimental neoplasms and non-random chromosome correlations in man. (1980) (27)
IDENTIFICATION OF ISOCHROMOSOME 17 IN ACUTE MYELOID LEUKÆMIA (1973) (27)
Aberrations of chromosome No. 1 in blastic phase of chronic myeloid leukemia. (2009) (27)
Multiple cytogenetic abnormalities in a case of osteosarcoma. (1986) (27)
Comparative cytogenetic and dna flow cytometric analysis of 150 bone and soft‐tissue tumors (1993) (27)
Cytogenetic analysis in the examination of solid tumors in children. (1994) (27)
The specificity of the chromosomal abnormalities in human colonic polyps. A cytogenetic study of multiple polyps in a case of Gardner's syndrome. (2009) (27)
Power law distribution of chromosome aberrations in cancer. (2003) (27)
Prognostic implications of cytogenetic aberrations in diffuse large B‐cell lymphomas (1999) (27)
Near-haploidy in two malignant fibrous histiocytomas. (1995) (27)
Unbalanced t(1;16) as the sole karyotypic abnormality in a breast carcinoma and its lymph node metastasis. (1994) (26)
Nonrandom secondary chromosome-aberrations in synovial sarcomas with t(x-18). (1995) (26)
Chromosome abnormalities in leiomyosarcomas. (1988) (26)
t(3;6;14)(p21;p21;q24) as the sole clonal chromosome abnormality in a hamartoma of the lung. (1992) (26)
Isochromosome 17 q in Blast Crisis of Chronic Myeloid Leukemia and in Other Hematologic Malignancies Is the Result of Clustered Breakpoints in 17 p 11 and Is Not Associated With Coding TP 53 Mutations (1999) (26)
Monosomy 22 in a case of biliary adenofibroma. (1997) (25)
The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas. (1997) (25)
Chromosomes of six primary sarcomas induced in the Chinese hamster by 7,12-dimethylbenz(a)anthracene. (2009) (25)
Disease‐associated patterns of disomic chromosomes in hyperhaploid neoplasms (2012) (25)
C-band pattern in lymphocytes of patients with soft tissue sarcomas. (1983) (25)
Predetermined sequential chromosome changes in serial transplantation of Rous rat sarcomas. (2009) (25)
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification. (2004) (24)
An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis. (1990) (24)
A 3q+ marker chromosome in EBV‐carrying nasopharyngeal carcinomas (1983) (24)
Proliferation-specific and differentiation-associated chromosomal breakpoints in human neoplasia--a unifying model. (2008) (24)
Highly malignant cells with normal karyotype in G-banding. (2009) (24)
No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24). (1989) (24)
Chromosomal evolution and tumor progression in a myxoid liposarcoma. (1990) (24)
Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndrome (1990) (24)
Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: A less complex karyotypic pattern? (1998) (23)
Cytogenetic study of pesticides in agricultural work. (2009) (23)
Occupational exposure to epoxy resins has no cytogenetic effect. (1980) (23)
Nineteen of 26 cellular oncogenes precisely localized in the human genome map to one of the 83 bands involved in primary cancer-specific rearrangements (1987) (23)
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia (2005) (23)
Another approach to in vivo estimation of genetic damage in humans. (1979) (23)
Cytogenetic studies in Hodgkin's disease. (2009) (23)
Multiple clonal chromosome aberrations in two thymomas. (1989) (23)
Nonrandom de novo chromosome aberrations in human lymphocytes and amniotic cells. (2008) (23)
Sister chromatid exchanges and structural chromosome aberrations in relation to age and sex (2004) (22)
Karyotypic characterization of bronchial large cell carcinomas (1994) (22)
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7). (1990) (22)
Biological effects in a chemical factory with mutagenic exposure (1988) (22)
Translocation 11;19 in a mucoepidermoid tumor of the lung. (1995) (22)
Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity (1998) (21)
Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha. (1996) (21)
Relationship between sister chromatid exchanges and structural chromosome aberrations in lymphocytes of 100 individuals. (1982) (21)
Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia. (1987) (21)
Chromosome analysis in 100 cases of first trimester trophoblast sampling (1985) (21)
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation (2002) (21)
Abstracts for the committee on the genetic constitution of chromosome 1 (1991) (21)
A case of myelodysplastic syndrome with high platelet counts and a t(3;8)(q26;q24). (1987) (21)
Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinoma. (1989) (21)
HYPERTENSION RELATED TO D.N.A. REPAIR SYNTHESIS AND CARCINOGEN UPTAKE (1975) (21)
Normal chromosome banding pattern in Alzheimer's disease. (1978) (20)
Nonrandom numerical chromosome abnormalities in basal cell carcinomas. (1998) (20)
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23) (2004) (20)
In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3–14.1 (1989) (20)
RT‐PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): Identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression (2002) (20)
Histologic—cytogenetic correlations in uterine leiomyomas (1991) (20)
High resolution analysis of the 5q-marker chromosome in refractory anemia. (2008) (20)
Trisomy 7 in nonneoplastic focal steatosis of the liver. (1992) (20)
Chromosomes in leukemia (1977) (20)
Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986‐91 (1997) (20)
Variable FHIT transcripts in non-neoplastic tissues. (1997) (20)
On the use of the Catalogue (1983) (20)
t(6;7)(q23;p22) as the sole chromosomal anomaly in a vocal cord carcinoma. (1988) (19)
Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8 (1997) (19)
Separate karyotypic features in a local recurrence and a metastasis of a fibrosarcoma. (1989) (19)
Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas. (1988) (19)
Structural chromosome aberrations in an adamantinoma. (1989) (19)
Relation between life expectancy and composition of the bone marrow at diagnosis of chronic myeloid leukaemia. (2009) (19)
Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality. (1990) (19)
Survival time in a population-based consecutive series of adult acute myeloid leukemia – the prognostic impact of karyotype during the time period 1976–1993 (2000) (19)
Clonal chromosome-aberrations in fibrocystic breast disease-associated with increased risk of cancer. (1994) (19)
Chromosome abnormalities identified by banding technique in a patient with acute myeloid leukaemia complicating Hodgkin's disease. (2009) (19)
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families (1996) (19)
Acute Myeloid Leukemia with inv(8)(p11q13) (2000) (19)
Cytogenetic abnormalities in an angioleiomyoma. (1989) (19)
Brief Communication: Abnormal Clones Resembling Those Seen in Blast CrisisArising in the Spleen in Chronic Myelocytic Leukemia (1975) (18)
Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign (2002) (18)
Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma. (1989) (18)
Comparison among five mutagenicity assays in workers producing polyurethane foams (1988) (18)
HL-A8 AND W15 IN DIABETES MELLITUS AND ESSENTIAL HYPERTENSION (1975) (18)
The relationship between growth in agar, karyotype and prognosis in acute leukaemia. (2009) (18)
Most gene fusions in cancer are stochastic events (2019) (18)
CHROMOSOME ABERRATIONS IN CHRONIC ALCOHOLICS (1978) (18)
Frequent rearrangement of chromosomal bands 1p22 and 11q13 in squamous cell carcinomas of the head and neck. (1991) (18)
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma. (2004) (18)
Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones. (1989) (18)
Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors. (1988) (17)
A model for karyotypic evolution in testicular germ cell tumors (2004) (17)
Metronidazole exhibits no clastogenic activity in a double-blind cross-over study on Crohn's patients. (2008) (17)
High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1 (1990) (17)
Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages. (1997) (17)
High resolution chromosome analysis of constitutional and acquired t(15;17) maps c-erbA to subband 17q11.2. (1986) (17)
Trisomy G-21 in adult myelomonocytic leukaemia. An abnormality common to granulocytic and monocytic cells. (2009) (17)
Second trimester prenatal diagnosis of the fragile X. (1986) (17)
Frequent miRNA-convergent fusion gene events in breast cancer (2017) (17)
Cytogenetic heterogeneity in a clear cell hidradenoma of the skin. (1994) (16)
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment‐related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15) (2002) (16)
Defective differentiation of megakaryocytes in acute myeloid leukemia. (2009) (16)
Trisomy 13 as a primary chromosome aberration in acute leukemia. (1991) (16)
14q+ marker chromosome in an EBV‐genome‐negative lymph node without signs of malignancy in a patient with EBV‐genome‐positive nasopharyngeal carcinoma (1979) (16)
Cytogenetic analysis in 941 consecutive patients with haematologic disorders. (2009) (16)
Translocation (2;3)(p21;p26) as the sole anomaly in a benign localized fibrous mesothelioma. (1996) (16)
CHROMOSOMES, LEUKÆMIA, AND OCCUPATIONAL EXPOSURE TO LEUKÆMOGENIC AGENTS (1979) (16)
Clustering of chromosomal breakpoints in neoplasia. (1986) (16)
Karyotypic abnormalities in adenocarcinomas of the lung. (1994) (16)
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia (1996) (15)
Relation between occupational exposure to organic solvents and chromosome aberrations in non‐Hodgkin's lymphoma (1989) (15)
Constitutional C-band pattern in patients with adenomatosis of the colon and rectum. (1985) (15)
DELETION OF THE LONG ARM OF CHROMOSOME 11 A Clinical Entity (1979) (15)
The chromosome territory of human oncogenes (1986) (14)
Comparative chromosome analysis of primary and metastatic Rous sarcomas in rats. (2009) (14)
Cytogenetic heterogeneity and clonal evolution in a recurrent fibrosarcoma (1993) (14)
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary. (1990) (14)
Near-haploidy in a case of plasmocytoma. (1986) (14)
Sister-chromatid exchanges in human lymphocytes after a non-S-phase incubation period to allow excision DNA repair-in vitro exposure to N-acetoxy-2-acetylaminofluorene and ethylene oxide. (1984) (14)
Telomeric location of retroviral oncogenes in humans. (2008) (14)
Molecular Characterization of 12 p Abnormalities in Hematologic Malignancies : Deletion of K I P I , Rearrangement of TEL , and Amplification of CCND 2 (2002) (14)
Chromosomal analysis of primary and metastatic Rous sarcomas in the rat. (2009) (14)
Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer. (1995) (14)
Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia. (1992) (14)
Cytogenetic analysis of six bronchial carcinoids. (1993) (14)
Cytogenetic damage as an endpoint in short-term assay systems for detecting environmental carcinogens. (1980) (14)
Near-haploid clones in a malignant fibrous histiocytoma. (1992) (14)
Differences in human C-band pattern between two European populations. (2008) (14)
Inversion inv(4)(p15q26) in a squamous cell carcinoma of the hypopharynx. (1988) (13)
G-band analysis in a serially transplanted Rous rat sarcoma. (2009) (13)
CORRELATION BETWEEN BLOOD-LEAD AND CHROMOSOMAL ABERRATIONS (1979) (13)
Fine needle aspiration biopsy: a useful tool in tumor cytogenetics with special reference to malignant lymphomas. (1981) (13)
Trisomy 7 in nonneoplastic kidney tissue cultured with and without epidermal growth factor. (1992) (12)
ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders (1998) (12)
Pronounced deficiency in T-cells and lymphocyte chromosomal aberrations in a patient with sarcoidosis, myelofibrosis and acute leukaemia following thorotrast angiography. (2009) (12)
Patterns of Chromosome Variation in Neoplasia (1990) (12)
Increased sister chromatid exchange frequency in chronic alcoholic users. (2008) (12)
First-trimester diagnosis on chorionic villi obtained by direct vision technique (2004) (12)
Karyotypic Characteristics of Colorectal Tumors (1997) (12)
Prenatal chromosomal analysis of fetal blood obtained at fetoscopy. (1980) (12)
Cytogenetically detected clonal heterogeneity in a duodenal adenocarcinoma. (1995) (12)
Involvement of 3p Deletions in Sporadic and Hereditary Forms of Renal Cell Carcinoma (1991) (12)
Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomas (1993) (12)
A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation. (1988) (12)
The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15. (1989) (11)
DO ONLY A FEW CHROMOSOMES CARRY GENES OF PRIME IMPORTANCE FOR MALIGNANT TRANSFORMATION? (1976) (11)
Characteristic patterns of chromosome abnormalities in acute myeloid leukemia with Auer rods. (1987) (11)
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation (2004) (11)
Cytogenetic findings in four malignant mixed mesodermal tumors of the ovary. (1996) (11)
Cytogenetic analysis of exocrine pancreatic carcinomas: Intratumor heterogeneity and nonrandom pattern of chromosome aberrations (1996) (11)
On the specificity of the G abnormality in human meningomas studied by the fluorescence technique. (2009) (11)
Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21). (1995) (11)
Chromosome pattern and survival in acute non-lymphocytic leukaemia in relation to age and occupational exposure to potential mutagenic/carcinogenic agents. (2009) (11)
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures. (2003) (11)
A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12. (1997) (11)
Cytogenetic and quantitative DNA analysis of primary and xenografted human osteosarcomas. (1989) (11)
Embryonal rhabdomyosarcoma with 100 chromosomes but no structural aberrations. (1992) (11)
TRENDS IN INCIDENCE OF ACUTE LEUKÆMIA (1979) (11)
No rearrangements of the CHOP gene in malignant fibrous histiocytoma. (1994) (11)
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families. (1996) (10)
The interrelations of micronuclei, chromosomal instability, and mutational activity in acute non-lymphocytic leukemia--a hypothesis. (2009) (10)
Chromosomes in neoplasia: An appeal for unpublished data (1979) (10)
The different origin of primary and secondary chromosome aberrations in cancer. (1981) (10)
Recurrent chromosomal imbalances in choroid plexus tumors. (1995) (10)
Comparative cytogenetic studies of bone marrow and extramedullary tissues in chronic myeloid leukemia. (1975) (10)
Telomeric association in a malignant fibrous histiocytoma (2004) (10)
Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma. (1998) (10)
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours (2005) (10)
Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland. (1995) (10)
Acute myeloid leukaemia with the Philadelphia chromosome. (2009) (10)
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia. (1988) (10)
A child with partial trisomy 7 and 20 inherited from the mother. (2009) (10)
Absence of late-replicating X-chromosome in a female patient with acute myeloid leukemia and the 8;21 translocation. (1979) (10)
Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma. (1988) (10)
Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas. (1998) (10)
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement. (1990) (10)
Abstracts for the committee on comparative gene mapping (1991) (9)
Mapping of the 19p13 breakpoint in an ovarian carcinoma between the INSR and TCF3 Loci (1993) (9)
Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis in a patient with Gardner's syndrome (1994) (9)
Chromosome abnormalities in solid tumors (1989) (9)
Late appearing 5q--marker in refractory anemia. (1987) (9)
The pathogenetic significance of acquired trisomy 8 is not reducible to amplification of a single chromosome band. (1995) (9)
Location of chromosome aberrations in bone marrow cells of individuals exposed mainly to petroleum vapors. (2009) (9)
Preface to Fourth Edition (2015) (9)
A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeres. (1995) (9)
Cytogenetic abnormalities in anin situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer (2005) (9)
Trends in incidence of acute leukaemia. (1979) (9)
Normal bone marrow karyotype in paroxysmal nocturnal hemoglobinuria--a cooperative European study. (1983) (8)
Chromosomes in Sipple's syndrome. (1973) (8)
Two unrelated clonal chromosome rearrangements in a nasal papilloma. (1989) (8)
Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging (1997) (8)
Cancer chromosome breakpoints cluster in gene‐rich genomic regions (2018) (8)
A twin study of structural chromosome aberrations in lymphocytes. (1986) (8)
Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary. (1993) (8)
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma. (1988) (8)
Chromosome aberrations and cytogenetic intratumor heterogeneity in chondrosarcomas (2005) (8)
Cytogenetic differences between bone marrow and spleen in a case of agnogenic myeloid metaplasia developing blast crisis. (2009) (7)
Cancer Cytogenetics: Heim/Cancer (2010) (7)
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia. (1991) (7)
ISCN (2005) is not acceptable for describing clonal evolution in cancer (2007) (7)
A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma. (1989) (7)
A twin study of sister chromatid exchanges in human lymphocytes following carcinogen exposure and DNA repair incubation. (1984) (7)
Cytogenetic and Molecular Genetic Evolution of Philadelphia-Chromosome-Positive Chronic Myeloid Leukaemia (2003) (7)
Prophase analysis of ring chromosome 13--an attempt at phenotype-karyotype correlation. (2009) (7)
Changes in the deoxyadenylate regions of rat DNA in sarcomas induced by 7,12-dimethylbenz(alpha)anthracene and Rous sarcoma virus. (2009) (7)
Clonal karyotypic evolution in a pediatric neurofibrosarcoma. (1995) (7)
Different cytogenetic patterns in skeletal breast cancer metastases (1996) (7)
Isochromosome 17q in a patient with acute myeloblastic leukemia. (1987) (7)
NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16) (2009) (7)
Genes, chromosomes & cancer: A new forum for research in cancer genetics (1989) (7)
Genetic changes in bone and soft tissue tumors. (1993) (7)
Isolation and regional localization of cosmid linking clones from human chromosome 12. (1994) (6)
Megaloblastic changes and chromosome abnormalities of erythropoietic cells in acute myeloid leukaemia. (1975) (6)
Chromosomal changes in cancer in relation to exposure to carcinogenic agents. (1984) (6)
Complex karyotype with an 11q13 homogeneously staining region in esophageal squamous cell carcinoma. (1995) (6)
Cancer cytogenetics update 2005 (2011) (6)
Trisomy 7 in non-neoplastic tubular epithelial cells of the kidney (1995) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Different chromosome morphology of diploid and aneuploid malignant cells. (1974) (6)
Morphometric analysis of sarcomas with different karyotypes. (1974) (6)
The significance of karyotypic changes in human neoplasia. (1987) (6)
A case of dysmyelopoietic syndrome with hypotetraploid karyotype. (1985) (6)
Relationship between cytogenetic findings and histopathology in non-Hodgkin lymphoma. (2009) (6)
Preferential chromosome loss in a Rous rat sarcoma in response to environmental changes. (2009) (6)
BCRABL‐negative chronic myeloid leukemia with ETV6ABL fusion (1997) (6)
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia. (1986) (6)
Normal bone marrow karyotype in acute leukemia or myelodysplasia following rheumatoid arthritis? (1987) (6)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Normal frequency of structural chromosome aberrations in fibroblasts from patients with non-Hodgkin's lymphoma. (2008) (5)
C-band polymorphism in non-Hodgkin lymphoma. (2008) (5)
Low mitotic activity of granulopoietic precursor cells in Ph1-chromosome-negative chronic myeloid leukaemia. (1974) (5)
Abstracts for the committee on the genetic constitution of chromosome 17 (1991) (5)
Transcriptomics paving the way for improved diagnostics and precision medicine of acute leukemia. (2021) (5)
Nonrandom chromosome abnormalities in cancer: An overview (2015) (5)
The absence of clastogenic effect during long-term and short-term treatment with metronidazole (1981) (5)
387 Chromosomal abnormalities involving 11Q13 are associated with poor prognosis in squamous cell carcinoma of the head and neck (1995) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
No FISH evidence for trisomy 7 in normal or leukemic bone marrow. (1996) (5)
NON-INDUSTRIAL EXPOSURE TO BENZENE AS LEUKÆMOGENIC RISK FACTOR (1977) (5)
Chromosome abnormalities in a carcinoma in pleomorphic adenoma of the lacrimal gland. (1991) (5)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3) (1991) (5)
Four cytogenetic subgroups can be identified in lipomas (1989) (5)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Abstracts for the committee on the genetic constitution of chromosome 2 (1991) (4)
Cytogenetic evaluation of bone marrow involvement in Burkitt's lymphoma. (1988) (4)
Relation between chromosomes and mitotic activity in acute myeloid leukemia. (2009) (4)
Rearrangement of chromosomal bands-3p13-14 in 2 hamartomas of the breast. (1995) (4)
Abnormal clones resembling those seen in blast crisis arising in the spleen in chronic myelocytic leukemia. (1975) (4)
Chromosome changes in cancer. (1986) (4)
Chromosomes, Auer rods and prognosis in acute myeloid leukaemia (1988) (4)
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22. (2008) (4)
Breakprone chromosome bands in fibroblasts from patients with non-Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non-Hodgkin's lymphomas. (2008) (4)
Abstracts for the committee on the genetic constitution of chromosome 6 (1991) (4)
Cytogenetic diagnosis of meningeal carcinomatosis. (1980) (4)
Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia. (2008) (4)
Abstracts for the committee on chromosomal changes in neoplasia (1991) (3)
Gardner's syndrome. (1973) (3)
Analysis of fusion transcripts indicates widespread deregulation of snoRNAs and their host genes in breast cancer (2020) (3)
Fourth International Workshop on Chromosomes in Leukemia 1982: Correlation of karyotype and occupational exposure to potential mutagenic/carcinogenic agents in acute nonlymphocytic leukemia. (1984) (3)
Cytogenetic analysis of pancreatic adenocarcinomas (1991) (3)
Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome. (1987) (3)
Abstracts for the committee on the genetic constitution of chromosome 12 (1991) (3)
Cancer: Chromosomal Abnormalities (2010) (3)
Isozyme patterns in Rous sarcoma virus-induced tumors in the rat. (2009) (3)
Do clonal chromosome abnormalities prognosticate early relapse in Hodgkin's disease? (1988) (3)
In situ hybridization localizes the human type II alpha 1 collagen gene (COL2A1) to 12q13. (2008) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Abstracts for the committee on the genetic constitution of chromosome 15 (1991) (3)
Pseudodiploid karyotypes in adenosquamous carcinomas of the lung. (1992) (3)
Relation between age and chromosomal aberrations at diagnosis of adult non-lymphocytic leukemia (1977) (3)
C-BAND HETEROMORPHOSM IN BREAST CANCER PATIENTS (1985) (2)
No cytogenic effect of metronidazole. (1980) (2)
Lysosomal enzymes in rat sarcomas induced by 7,12-dimethylbenz(alpha)anthracene and Rous sarcoma virus. (2009) (2)
Abstracts for the committee on the genetic constitution of chromosome 11 (1991) (2)
Erratum: Improved technique for short-term culture and cytogenetic analysis of human breast cancer (Genes Chrom Cancer 5:14-20, (1992)) (1992) (2)
The origin of double-minutes in a Rous rat sarcoma. (2009) (2)
Different cytogenetic patterns in skeletal breast cancer metastases. (1996) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Cytogenetic and molecular genetic evolution of Phi (2003) (2)
Clinical Significance of Cytogenetic Findings in Solid Tumors (1997) (2)
What is the Significance of Chromosome Aberrations in Malignant Cells (1981) (2)
Acute myeloid leukemia (AML-M1) with multiple trisomies and t(8;21)(q22;q22). (1994) (2)
Abstracts for the committee on the genetic constitution of chromosome 16 (1991) (2)
Isozymes of experimentally induced primary sarcomas in the rat. (2009) (2)
No abnormal C-band polymorphism in lung cancer patients. (2008) (2)
Cytogenetic analysis of basal cell carcinoma (1991) (2)
How it all began (2015) (2)
Abstracts for the committee on the genetic constitution of chromosome 22 (1991) (2)
Abstracts for the committee on the genetic constitution of chromosome 13 (1991) (1)
The human cancer chromosome registry — An update (1991) (1)
Letter: Identification of isochromosome 17 in acute myeloid leukaemia. (1973) (1)
Detection of recurrence and clonal evolution of ANLL-M4 by high resolution banding analysis of the unique reciprocal translocation t(6;9) in a teenager girl (1986) (1)
Clinical impact of solid tumor cytogenetics (1996) (1)
Cytogenetic intra-tumor heterogenetty in three large sarcomas (1991) (1)
Application of cytogenetic methods to analysis of etiologic factors in carcinogenesis. (1982) (1)
83 The specific translocation t(12;14)(q14–15;q23–24) and other clonal chromosome rearrangements in 20 uterine leiomyomas (1989) (1)
[Cytogenetic diagnosis of tumors. Clinical significance of chromosome aberrations]. (1997) (1)
Abstracts for the committee on the genetic constitution of the Y chromosome (1991) (1)
The human cancer chromosome registry (1989) (1)
Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients (1988) (1)
Clonal chromosome abnormalities in two chemodectomas. (1996) (1)
Clonal chromosome abnormalities in two chemodectomas (1996) (1)
Tumors of the skin (2015) (1)
Subject Index Vol. 52, 1989 (1989) (1)
A comparative morphologic study of Rous rat sarcoma with normal and abnormal chromosomal pattern. (1972) (1)
Gene Expression Profiling of Leukemic Cell Lines and Primary Leukemias Reveals Conserved Molecular Signatures among Subtypes with Specific Genetic Aberrations: Identification of Fusion Gene-Specific Transcriptional Profiles and Expression Pattern of Tyrosine Kinase-Encoding Genes. (2004) (1)
Abstracts for the committee on the genetic constitution of chromosome 7 (2004) (1)
Abstracts for the committee on the genetic constitution of chromosome 4 (1991) (1)
Abstracts for the committee on the genetic constitution of chromosome 10 (1991) (1)
Response to letter by the ISCN standing committee (2007) (1)
Abstracts for the committee on the genetic constitution of chromosome 9 (1991) (1)
Trisomy 12 is a consistent chromosomal change in benign tumors of the ovary (1991) (1)
Cancer cytogenetics: Fourth edition (2015) (1)
Contents Vol. 55, 1990 (1990) (1)
Consistent occurrence of 19+ marker chromosomes in ovarian seropapillary cystadenocarcinomas (1991) (1)
Contents, Vol. 19, 1977 (1977) (0)
Deletions of 3p in breast tumors (1996) (0)
Karyotypic characteristics of uterine leiomyoma (1991) (0)
Genetic Convergence and Divergence in Tumor Progression 1 (2006) (0)
Abstractsfor the DNA committee (1991) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Abstracts for the committee on the genetic constitution of chromosome 21 (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 8 (1991) (0)
Index of GDB source ID numbers (1991) (0)
1018 Cytogenetics of mesenchymal tumors (1995) (0)
Chromosome Aberration in Human Neoplasm: Occurrence and Significance (2008) (0)
Abstracts dscribing resources, technological and other developments (1991) (0)
Chromosome analysis guidelines - preliminary report (2016) (0)
Karyotypic aberrations in an anal-canal malignant-melanoma and its local metastasis. (1995) (0)
The banding pattern in Philadelphia‐chromosome negative chronic myeloid leukemia (2009) (0)
3. Cytogenetic nomenclature (2015) (0)
Cytogenetic multiclonality in primary breast carcinomas (1992) (0)
Cytogenetic comparisons of colorectal metalpastic polyps, adenomas, and carcinomas: Karyotypic evidence for a common clonal origin in some patients (1996) (0)
Chromosome Aberrations, Tumor-Specific (2002) (0)
Multiple cytogenetically unrelated clones in short-term cultures from squamous cell carcinomas (1989) (0)
Structural and numerical chromosome changes in colorectal cancer develop through telomere-mediated anaphase bridging and not through mitotic multipolarity " (2005) (0)
Cytogenetic analysis of adenocarcinomas of the lung (1994) (0)
Abstracts for the committee on the genetic constitution of chromosome 18 (1991) (0)
A new approach to an old problem. (2010) (0)
15 The cancer chromosome registry - solid tumors (1992) (0)
Abstract Oral presentationThe human cancer chromosome registry (1989) (0)
Contents, Vol. 52, 1989 (1989) (0)
Cytogenetic analysis of 206 large bowel tumors: evidence of pathogenetic heterogeneity during colorectal carcinogenesis (1995) (0)
Abstracts for the committee on linkage and gene order (1991) (0)
Introduction to special issue for Alfred G. Knudson (2003) (0)
Abstracts for the committee on the genetic constitution of chromosome 20 (1991) (0)
Amplification of INT1 in retinoblastomas (1989) (0)
Admixture of intact or lysed platelets to lymphocyte cultures results in higher chromosome aberration frequencies. (2008) (0)
Frequent miRNA-convergent fusion gene events in breast cancer (2017) (0)
Influence of choice of tissue culture technique on karytotypic pattern in head and neck squamous cell carcinomas (1992) (0)
Abstractsfor the informatics committee (1991) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Cytogenetic markers of host susceptibility in carcinogenesis. (1983) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
[Chromosome deviations in hematological diseases]. (1983) (0)
Index by Keyword (1989) (0)
The prognostic implication of cytogenetic findings in non‐Hodgkin lymphomas (1986) (0)
Micronuclei in Cultured Lymphocytes as an Indicator of Genotoxic Exposure (1984) (0)
Chromosomal segments of critical significance in human neoplasia. (1986) (0)
Evidence for a Single Step Mechanism in the Origin of Hyperdiploid Childhood Acute Lymphoblastic Leukemia. (2004) (0)
Secondary chromosome aberrations in synovial sarcoma with t(X;18) (1995) (0)
AbstractFour cytogenetic subgroups can be identified in lipomas (1989) (0)
Index by Abstract Number (1989) (0)
Cytogenetically unrelated clones in pancreatic carcinomas (1994) (0)
Letter: HL-A8 and W15 in diabetes mellitus and essential hypertension. (1975) (0)
Chop in liposarcoma, variations on a theme (1996) (0)
Abstracts for the committee on clinical disorders and chromosomal deletion syndromes (1991) (0)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 2 of 3) (2004) (0)
18 Different cytogenetic subgroups among benign lipogenic tumors (1987) (0)
Author Index / Subject Index Vol. 49, 1988 (1988) (0)
Pseudo- and neardiploid karyotypes in adenosquamous carcinomas of the lung (1991) (0)
Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis and a cell line established from the metastasis in a patient with Gardner's syndrome. (1994) (0)
Two variants of the TLS-CHOP fusion transcript in myxoid liposarcomas with the 12;16 translocation (1994) (0)
[The clinical significance of chromosome study in leukemia]. (1975) (0)
A cytogenetical analysis in patients with secondary hematological disorders. (1987) (0)
Samuel A. Latt, 1938–1988 (1988) (0)
EWS and FUS/TLS related genes (1996) (0)
Editorial (1990) (0)
[Significance of chromosomal abnormalities in solid tumors of humans]. (1994) (0)
[Scientific fraud--the journals' dilemma]. (2004) (0)
Cytogenetic aberrations in colorectal carcinomas and their correlation with survival (1992) (0)
Cytogenetic evidence of polyclonality in epithelial tumors (1997) (0)
Chromosome 5 abnormalities in large cell carcinomas of the lung (1992) (0)
Acute lymphocytic and myelomonocytic leukemia associated with low platelet counts and a 21q- marker chromosome (2004) (0)
Abstracts for the committee on the genetic constitution of chromosome 14 (1991) (0)
Mammary carcinogenesis in cytogenetic perspective: chromosome abnormalities in 207 breast tumors (1995) (0)
Chromosome abnormalities in mesenchymal neoplasms (1986) (0)
107 Clonal chromosome aberrations in two thymomas (1989) (0)
[Chromosome changes and cancer]. (1973) (0)
Cytogenetic analysis of colon carcinomas (1991) (0)
Cytogenetic Analysis of 33 Basal Cell Carcinomas 1 (2006) (0)
Subject Index, Vol. 69, 1995 (2004) (0)
Farewell message from the Editor‐in‐Chief of Genes, Chromosomes & Cancer (2020) (0)
46 Ring chromosomes in soft tissue tumors (1987) (0)
Abstracts for the comparative subcommittee on human and mouse homologies (1991) (0)
Recurrent chromosome abnormalities in solid tumors (1995) (0)
Giemsa‐negative chromosome bands preferentially recombine in cancer‐associated translocations and gene fusions (2022) (0)
A cloud-based resource for genome coordinate-based exploration and large-scale analysis of chromosome aberrations and gene fusions in cancer. (2023) (0)
The mullerian-inhibiting substance gene is transcribed in human ovarian carcinomas with and without 19p rearrangements. (1994) (0)
Announcement (1992) (0)
Abstracts for the committee on the mitochondrial genome (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 19 (1991) (0)
Subject Index Vol. 19, 1977 (1977) (0)
Characteristic karyotypic features in non-squamous cell carcinomas of the head and neck (1994) (0)
Subject Index Vol. 58, 1991 (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 5 (1991) (0)
10 Multiple cytogenetic clones in squamous cell carcinomas (1989) (0)
Advances in Brief Power Law Distribution of Chromosome Aberrations in Cancer 1 (2003) (0)
The vanding pattern in philadelphia-chromosome negative chronic myeloid leukemia. (1974) (0)
Deoxyribonucleic acid repair synthesis: a new factor for defining high blood pressure. (1976) (0)
Chromosome translocations and cancer (2015) (0)
[Diagnostic biopsy of the chorion at Lund Hospital]. (1983) (0)
Cancer Chromosomes: From Meaningless Noise to Proof of Principle. (2009) (0)

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