Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients

Cancer Genetics and Cytogenetics

Volumn 92, Issue 2, 1996, Pages 111-115

  Heerema, Nyla A ^a   Maben, Kathleen D ^a   Bernstein, Jonathan ^a   Breitfeld, Philip P ^a   Neiman, Richard S ^a   Vance, Gail H ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMMON ACUTE LYMPHOBLASTIC LEUKEMIA ANTIGEN;

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; BONE MARROW BIOPSY; CANCER RECURRENCE; CANCER REGRESSION; CASE REPORT; CHILD; CHROMOSOME 20; CHROMOSOME 9; CLINICAL FEATURE; CYTOGENETICS; DICENTRIC CHROMOSOME; FLOW CYTOMETRY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOPHENOTYPING; KARYOTYPE; PRIORITY JOURNAL;

ADULT; BONE MARROW; CENTROMERE; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 9; FOLLOW-UP STUDIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INTERPHASE; KARYOTYPING; LEUKEMIA, B-CELL, ACUTE; LEUKEMIA, PRE-B-CELL; TIME FACTORS; TRANSLOCATION, GENETIC;

EID: 0030465498     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00172-0     Document Type: Article

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