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Paper Details

Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.
Mol Genet Genomic Med
10
2015
/MIR3922 deletion, 55 kb region, CHST11, CHST11 deficiency, MIR3922, carbohydrate, chondrodysplasia, chondroitin-4-sulfotransferase 1, chromosome 12q23, congenital limb malformation, disaccharide, human, limb malformation, malignant lymphoproliferative disease, mice, microRNA, skeletal malformation, tumor
Author NameAffiliation
Ignaty LeshchinerBroad Institute, Brigham and Women's Hospital Cambridge
Chengsheng Zhang
Nathan O StitzielWashington University School of Medicine St. Louis
Matthew S LeboPartners Healthcare Center for Personalized Medicine Cambridge
Heidi L RehmPartners Healthcare Center for Personalized Medicine Cambridge
Heidi L RehmPartners Healthcare Center for Personalized Medicine Cambridge
Richard L MaasBrigham and Women's Hospital, Harvard Medical School Boston
Shamil R SunyaevBrigham and Women's Hospital, Harvard Medical School Boston
Shamil R SunyaevBrigham and Women's Hospital, Harvard Medical School Boston
Michael F MurrayDana Farber Cancer Institute, Brigham and Women's Hospital Boston
Michael F MurrayDana Farber Cancer Institute, Brigham and Women's Hospital Boston
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