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Publications by Michael A. Simpson
Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome
American Journal of Human Genetics
Genetics
De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome
American Journal of Human Genetics
Genetics
Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-B in Inherited Skin Fragility
American Journal of Human Genetics
Genetics
