In non-follicular lymphoproliferative disorders, IGH/BCL2-fusion is not restricted to chronic lymphocytic leukaemia

British Journal of Haematology

Volumn 158, Issue 4, 2012, Pages 489-498

  Baseggio, Lucile ^a,b   Geay, Marie Odile ^a,b   Gazzo, Sophie ^a,b   Berger, Françoise ^a,b   Traverse Glehen, Alexandra ^a,b   Ffrench, Martine ^a,b   Hayette, Sandrine ^a,b   Callet Bauchu, Evelyne ^a,b   Verney, Aurélie ^b   Morel, Dominique ^a,b   Jallades, Laurent ^a,b   Magaud, Jean Pierre ^a,b   Salles, Gilles ^a,b,c   Felman, Pascale ^a,b  

^a CENTRE HOSPITALIER LYON SUD   (France)

^b UNIVERSITÉ LYON 1   (France)

^c HOSPICES CIVILS DE LYON   (France)

Author keywords

Chronic lymphocytic leukaemia; FISH; IGHV; Immunophenotype; Marginal zone lymphoma; T(14; 18)

Indexed keywords

ANTINEOPLASTIC AGENT; BETA 2 MICROGLOBULIN; CYCLOPHOSPHAMIDE; DOXORUBICIN; GENOMIC DNA; LACTATE DEHYDROGENASE; PREDNISOLONE; RITUXIMAB; VINCRISTINE;

ADULT; AGED; ANEMIA; ARTICLE; BCL2 GENE; BCL6 GENE; CANCER COMBINATION CHEMOTHERAPY; CANCER IMMUNOTHERAPY; CHRONIC B CELL LYMPHOPROLIFERATIVE DISEASE; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; CLINICAL FEATURE; CYTOGENETICS; DISEASE SEVERITY; FAS GENE; FEMALE; FLOW CYTOMETRY; GENE FUSION; GENE LOCUS; GENE MUTATION; GENE TRANSLOCATION; HISTOGENESIS; HUMAN; HUMAN TISSUE; IGH GENE; IGHV GENE; IMMUNOHISTOCHEMISTRY; IMMUNOPHENOTYPING; LYMPH NODE BIOPSY; LYMPHADENOPATHY; LYMPHOCYTE COUNT; LYMPHOCYTOMA; LYMPHOPROLIFERATIVE DISEASE; MALE; MANTLE CELL LYMPHOMA; MONOCLONAL B CELL LYMPHOCYTOSIS; MORPHOLOGY; ONCOGENE; OUTCOME ASSESSMENT; OVERALL SURVIVAL; PRIORITY JOURNAL; PROLYMPHOCYTE; PROTEIN BLOOD LEVEL; SEQUENCE HOMOLOGY; SPLENIC MARGINAL ZONE LYMPHOMA; SPLENOMEGALY; THROMBOCYTOPENIA;

CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 18; GENES, BCL-2; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; IMMUNOPHENOTYPING; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; LYMPHOCYTOSIS; LYMPHOPROLIFERATIVE DISORDERS; MALE; MIDDLE AGED; ONCOGENE FUSION; TRANSLOCATION, GENETIC; TREATMENT OUTCOME; TRISOMY;

EID: 84864319942     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2012.09178.x     Document Type: Article

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