Search Results - Raynaud, S.D.

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  1. 1
    Fluorescence in Situ Hybridization Analysis of t(3; 12)(q26;p13): A Recurring Chromosomal Abnormality Involving the TEL Gene (ETV6) in Myelodysplastic Syndromes

    Fluorescence in Situ Hybridization Analysis of t(3; 12)(q26;p13): A Recurring Chromosomal Abnormality Involving the TEL Gene (ETV6) in Myelodysplastic Syndromes by Raynaud, S.D., Baens, M., Grosgeorge, J., Rodgers, K., Reid, C.D.L., Dainton, M., Dyer, M., Fuzibet, J.G., Gratecos, N., Taillan, B., Ayraud, N., Marynen, P.

    Published in Blood
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    Identification of Epigenetically Silenced Tumor Suppressor Genes in Myeloid Disorders Leads to the Identification of α-Catenin as a Target Gene in 5q- Syndrome

    Identification of Epigenetically Silenced Tumor Suppressor Genes in Myeloid Disorders Leads to the Identification of α-Catenin as a Target Gene in 5q- Syndrome by Desmond, J.C., Raynaud, S.D., Jones, L.C., Hofmann, W.K., Haferlach, T., Koeffler, H. Phillip

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  3. 3
    Place de la cytogénétique dans la prise en charge des syndromes myélodysplasiques primaires

    Place de la cytogénétique dans la prise en charge des syndromes myélodysplasiques primaires by Raynaud, S.D

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