Exome sequencing identifies recurrent BCOR alterations and the
Exome sequencing identifies recurrent BCOR alterations and the absence of KLF 2, TNFAIP 3 and MYD 88 mutations in splenic diffuse red pulp small B-cell lymphoma by Laurent Jallades, Lucile Baseggio, Pierre Sujobert, Sarah Huet, Kaddour Chabane, Evelyne Callet-Bauchu, Aurélie Verney, Sandrine Hayette, Jean-Pierre Desvignes, David Salgado, Nicolas Levy, Christophe Béroud, Pascale Felman, Françoise Berger, Jean-Pierre Magaud, Laurent Genestier, Gilles Salles, and Alexandra Traverse-Glehen haematol Volume 102(10): 1758 -1766 September 30, 2017 © 2017 by Ferrata Storti Foundation
Clinico-pathological comparison between the HCL, SDRPL and SMZL cases of our series. Laurent Jallades et al. Haematologica 2017; 102: 1758 -1766 © 2017 by Ferrata Storti Foundation
Distribution of mutations in hairy-cell leukemia, splenic diffuse red pulp lymphoma and splenic marginal zone lymphoma. Laurent Jallades et al. Haematologica 2017; 102: 1758 -1766 © 2017 by Ferrata Storti Foundation
BCOR mutations in splenic diffuse red pulp lymphoma, lymphoid and hematologic malignancies. Laurent Jallades et al. Haematologica 2017; 102: 1758 -1766 © 2017 by Ferrata Storti Foundation
Copy number evaluation at the BCOR Xp 11. 4 locus in hairy-cell leukemia, splenic diffuse red pulp lymphoma and splenic marginal zone lymphoma. Laurent Jallades et al. Haematologica 2017; 102: 1758 -1766 © 2017 by Ferrata Storti Foundation
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