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  1. No Access

    Article

    The 5th edition of the WHO classification of haematolymphoid tumors: comments from the Groupe Francophone de Cytogénétique Hématologique (GFCH)

    Florence Nguyen-Khac, Audrey Bidet, Marie-Bérengère Troadec, Lauren Veronese… in Leukemia (2023)

  2. No Access

    Article

    Recommendations for cytogenomic analysis of hematologic malignancies: comments from the Francophone Group of Hematological Cytogenetics (GFCH)

    Florence Nguyen-Khac, Audrey Bidet, Lauren Veronese, Agnes Daudignon… in Leukemia (2020)

  3. No Access

    Article

    Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy

    Estelle Balducci, Vanessa Nivaggioni, John Boudjarane… in Annals of Hematology (2017)

  4. Article

    Open Access

    First case of B ALL with KMT2A-MAML2 rearrangement: a case report

    A large number of chromosomal translocations of the human KMT2A gene, better known as the MLL gene, have so far been characterized. Genetic rearrangements involving KMT2A gene are frequently involved in lymphoid,...

    Estelle Menu, Nathalie Beaufils, Fabrice Usseglio, Estelle Balducci… in BMC Cancer (2017)

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  5. No Access

    Article

    Identification of new classes among acute myelogenous leukaemias with normal karyotype using gene expression profiling

    Conventional cytogenetic analysis currently stratifies acute myelogenous leukaemia (AML) into prognostically relevant groups. However, approximately 50% of adult AMLs have normal cytogenetics (NC-AMLs), and re...

    Norbert Vey, Marie-Joëlle Mozziconacci, Agnès Groulet-Martinec, Stéphane Debono… in Oncogene (2004)

  6. No Access

    Article

    Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

    The inv(16) and related t(16;16) are found in 10% of all cases with de novo acute myeloid leukemia. In these rearrangements the core binding factor β (CBFB) gene on 16q22 is fused to the smooth muscle myosin heav...

    Bert A van der Reijden, Hans G Dauwerse, Rachel H Giles… in Oncogene (1999)

  7. No Access

    Article

    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

    A stem-cell myeloproliferative disorder involving T- and B-cell, and myeloid lineages, is associated with three different translocations with a breakpoint in region p11-12 of chromosome 8: t(6;8)(q27;p11), t(8...

    Max Chaffanet, Cornel Popovici, Dominique Leroux, Michèle Jacrot, José Adélaïde… in Oncogene (1998)

  8. No Access

    Article

    Human CD28 and CTLA-4 Ig superfamily genes are located on chromosome 2 at bands q33–q34

    CD28 is a cell surface molecule present on most peripheral T cells which has been implied in the amplification of the T-cell response in vitro. Using in situ hybridization on human prometaphase cells, we have ...

    Marina Lafage-Pochitaloff, Régis Costello, Dominique Couez… in Immunogenetics (1990)