Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: A new recurring and cryptic abnormality

Leukemia

Volumn 16, Issue 1, 2002, Pages 7-12

  Helias C ^a   Leymaire, V ^a   Entz Werle, N ^b   Falkenrodt, A ^a   Eyer, D ^b   Costa, J A ^c   Cherif, D ^c   Lutz, P ^b   Lessard, M ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^b HÔPITAL DE HAUTEPIERRE   (France)

^c Genset SA   (France)

Author keywords

IPM FISH; T cell ALL; t(5; 14)(q35; q32)

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; CASE REPORT; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME 14Q; CHROMOSOME 5Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME PAINTING; CHROMOSOME TRANSLOCATION 14; CHROMOSOME TRANSLOCATION 5; CONTROLLED STUDY; DNA HYBRIDIZATION; DNA RESTRICTION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE SEQUENCE; HUMAN; HUMAN TISSUE; INTERMETHOD COMPARISON; KARYOTYPE; MALE; MOLECULAR PROBE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECURRENT DISEASE; T CELL LEUKEMIA; TELOMERE; VALIDATION PROCESS;

EID: 85009836740     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2402347     Document Type: Article

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