Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: Rearrangements of DNA satellite II and new recurrent translocations

Leukemia

Volumn 13, Issue 12, 1999, Pages 1975-1981

  Busson Le Coniat, M ^a   Salomon Nguyen, F ^a   Dastugue, N ^b   Maarek, O ^c   Lafage Pochitaloff, M ^d   Mozziconacci, M J ^d   Baranger, L ^e   Brizard, F ^f   Radford, I ^g   Jeanpierre, M ^h   Bernard, O A ^a   Berger, R ^a  

^a INSERM   (France)

^b CHU PURPAN   (France)

^c Laboratoire Central d'Hematologie   (France)

^d INSTITUT PAOLI CALMETTES   (France)

^e ANGERS UNIVERSITY HOSPITAL   (France)

^f POITIERS UNIVERSITY HOSPITAL   (France)

^g HÔPITAL NECKER ENFANTS MALADES   (France)

^h Hop Cochin Maternités ^*  (France)

Author keywords

Chromosome 1; Hematopoietic disorders; Recurrent translocation; Satellite DNA

Indexed keywords

SATELLITE DNA;

ACUTE LEUKEMIA; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 1Q; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 16; CHROMOSOME TRANSLOCATION 2; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROCHROMATIN; HUMAN; MALE; PRIORITY JOURNAL;

EID: 0032756052     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2401587     Document Type: Article

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