Loss of 17p is a major consequence of whole-arm chromosome translocations in hematologic malignancies

Cancer Genetics and Cytogenetics

Volumn 173, Issue 2, 2007, Pages 136-143

  Adeyinka, Adewale ^a   Wei, Sainan ^a   Sanchez, Jessica ^a  

^a HENRY FORD HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCENTRIC CHROMOSOME; ADULT; AGED; ARTICLE; CHROMOSOME 1; CHROMOSOME 11; CHROMOSOME 16; CHROMOSOME 17P; CHROMOSOME 19; CHROMOSOME 1Q; CHROMOSOME 2; CHROMOSOME 20; CHROMOSOME 3; CHROMOSOME 4; CHROMOSOME 6; CHROMOSOME 7; CHROMOSOME ARM; CHROMOSOME TRANSLOCATION 17; CLONAL VARIATION; CONTROLLED STUDY; CYTOGENETICS; DATA BASE; DIPLOIDY; DISEASE COURSE; FEMALE; GENETIC ASSOCIATION; HEMATOLOGIC MALIGNANCY; HUMAN; HUMAN CELL; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROGNOSIS; ROBERTSONIAN CHROMOSOME TRANSLOCATION; STATISTICAL SIGNIFICANCE; X CHROMOSOME; Y CHROMOSOME;

ADULT; AGED; AGED, 80 AND OVER; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HEMATOLOGIC NEOPLASMS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MIDDLE AGED; TRANSLOCATION, GENETIC;

ROBERTSONIA;

EID: 33847132734     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2006.10.013     Document Type: Article

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