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MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4

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Bibliographic Details
Published in:	Haematologica (Roma) 2018-09, Vol.103 (9), p.e408-e411
Main Authors:	Guerrera, Maria Luisa, Tsakmaklis, Nickolas, Xu, Lian, Yang, Guang, Demos, Maria, Kofides, Amanda, Chan, Gloria G, Manning, Robert J, Liu, Xia, Chen, Jiaji G, Munshi, Manit, Patterson, Christopher J, Castillo, Jorge J, Dubeau, Toni, Gustine, Joshua, Carrasco, Ruben D, Arcaini, Luca, Varettoni, Marzia, Cazzola, Mario, Treon, Steven P, Hunter, Zachary R
Format:	Article
Language:	English
Subjects:	Biomarkers Chromosome Deletion Genetic Association Studies Humans Mutation Myeloid Differentiation Factor 88 - genetics Online Only Receptors, CXCR4 - genetics Waldenstrom Macroglobulinemia - diagnosis Waldenstrom Macroglobulinemia - genetics
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