Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q

Cancer Genetics and Cytogenetics

Volumn 173, Issue 2, 2007, Pages 144-149

  Smoley, Stephanie A ^a   Fink, Stephanie R ^a   Paternoster, Sarah F ^a   Stockero, Kimberly J ^a   Nguyen, Lai P ^a   Nguyen, Phuong L ^a   Hanson, Curtis A ^a   Dewald, Gordon W ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; BLOOD; BONE MARROW; CELL CYCLE ARREST; CHROMOSOME 20Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENETIC VARIABILITY; HUMAN; HUMAN CELL; INTERPHASE; KARYOTYPE; MALE; MARKER CHROMOSOME; METAPHASE; MONOSOMY; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; PATHOLOGY; PRIORITY JOURNAL;

ACUTE DISEASE; AGED; AGED, 80 AND OVER; CENTROMERE; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; HEMATOLOGIC DISEASES; HUMANS; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES;

EID: 33847099585     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2006.11.003     Document Type: Article

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