t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

Oncogene

Volumn 16, Issue 7, 1998, Pages 945-949

  Chaffanet, Max ^a,b   Popovici, Cornel ^a   Leroux, Dominique ^c   Jacrot, Michèle ^c   Adélaïde, José ^b   Dastugue, Nicole ^d   Grégoire, Marie José ^e   Hagemeijer, Anne ^f   Lafage Pochitaloff, Marina ^a,g   Birnbaum, Daniel ^a,b   Pébusque, Marie Josèphe ^a  

^a INSERM   (France)

^b INSTITUT PAOLI CALMETTES   (France)

^c INSTITUT ALBERT BONNIOT   (France)

^d CHU PURPAN   (France)

^e UNIVERSITY HOSPITAL OF NANCY   (France)

^f UNIVERSITY OF LEUVEN   (Belgium)

^g IPC   (France)

Author keywords

FGFR1 gene; Fluorescence; Hematopoiesis; Human chromosome pairs 6, 8, 9, 13; In situ hybridization; Leukemia; Lymphoma; Stem cell; Translocation

Indexed keywords

FIBROBLAST GROWTH FACTOR;

ADULT; ARTICLE; B LYMPHOCYTE; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 6; CHROMOSOME TRANSLOCATION 8; COSMID; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; SOUTHERN BLOTTING; STEM CELL; T LYMPHOCYTE;

EID: 14444277275     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1201601     Document Type: Article

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