Inherited <i>CHST11/MIR3922</i> deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease
Sameer S. Chopra(Harvard University), Christopher A. Cassa(Brigham and Women's Hospital), Heidi L. Rehm(Unknown), Robin Joyce(Beth Israel Deaconess Medical Center), Heather M. McLaughlin, Monica A. Giovanni(Brigham and Women's Hospital), Michael F. Murray(Brigham and Women's Hospital), Ignaty Leshchiner(Broad Institute), Hatice Duzkale(Yeditepe University), Shamil Sunyaev(Harvard University), Nathan O. Stitziel(Amgen (United States)), Matthew S. Lebo(Brigham and Women's Hospital), Chengsheng Zhang(Nanchang University), Joyce D. Fingeroth(Beth Israel Deaconess Medical Center), Richard L. Maas(Brigham and Women's Hospital), Dana Vuzman
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