13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation

Cancer Genetics and Cytogenetics

Volumn 174, Issue 2, 2007, Pages 151-160

  Struski, Stephanie ^a   Helias, Catherine ^a   Gervais, Carine ^a   Audhuy, Bruno ^b   Zamfir, Alina ^a   Herbrecht, Raoul ^a   Lessard, Michel ^a  

^a HÔPITAL DE HAUTEPIERRE   (France)

^b Hôpitaux Civils de Colmar   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ANALYTIC METHOD; ARTICLE; B CELL LYMPHOMA; CENTROMERE; CHROMOSOME 13Q; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INTERPHASE; LYMPHOPROLIFERATIVE DISEASE; MALE; METAPHASE; PRIORITY JOURNAL; TELOMERE;

AGED; CHROMOSOME BANDING; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, B-CELL, CHRONIC; LYMPHOMA, SMALL-CELL; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 34247181068     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2006.12.004     Document Type: Article

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