Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21 q, 11q, and 22q

Genes Chromosomes and Cancer

Volumn 34, Issue 2, 2002, Pages 137-153

  Mrózek, Krzysztof ^a   Heinonen, Kristiina ^a,c   Theil, Karl S ^b   Bloomfield, Clara D ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b OHIO STATE UNIVERSITY   (United States)

^c KUOPIO UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; CHROMOSOME 11Q; CHROMOSOME 21Q; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE OVEREXPRESSION; GENETIC ANALYSIS; HUMAN; KARYOTYPING; LEUKEMOGENESIS; MALE; PRIORITY JOURNAL;

ACUTE DISEASE; ADULT; AGED; AGED, 80 AND OVER; ALLELIC IMBALANCE; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED;

EID: 0036262776     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.10027     Document Type: Article

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