Detection of 11q13 rearrangements in hematologic neoplasias by double-color fluorescence in situ hybridization

Blood

Volumn 87, Issue 4, 1996, Pages 1512-1519

  Coignet, Lionel J A ^a   Schuuring, Ed ^a   Kibbelaar, Robby E ^a   Raap, Ton K ^a   Kleiverda, Karin K ^a   Bertheas, Marie Françoise ^a   Wiegant, Joop ^a   Beverstock, Geoffrey ^a   Kluin, Philip M ^a  

^a Department of Pathology ^*

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 11Q; CHROMOSOME 14; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 11; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; CONTROLLED STUDY; COSMID; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; INTERPHASE; MALE; METAPHASE; PRIORITY JOURNAL;

ADULT; AGED; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 14; COSMIDS; CYCLIN D1; DNA, NEOPLASM; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHOMA, SMALL CLEAVED-CELL, DIFFUSE; MALE; MIDDLE AGED; PROTO-ONCOGENE PROTEINS; TRANSLOCATION, GENETIC;

EID: 0030058567     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v87.4.1512.bloodjournal8741512     Document Type: Article

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