William R. Wilcox, MD, PhD is Director of the Metabolic Disorders Clinic in Medical Genetics and Director of the Skeletal Dysplasia Morphology Laboratory at Cedars-Sinai. Dr. Wilcox also serves Cedars-Sinai as Director of the Lysosomal Storage Disease Treatment and Research Center, Residency Director for the Medical Genetics Residency and Assistant Professor of the Medical Genetics Fellowship Program.
Dr. Wilcox is board certified in pediatrics, clinical genetics, clinical biochemical genetics and clinical molecular genetics. His current research interests include enzyme replacement in lysosomal storage diseases; the morphology, genetics and pathophysiology of human dwarfing conditions (skeletal dysplasias); and identification of the genetic defect in the Marinesco-Sjögren syndrome. He is on the advisory board of the Fabry Disease Registry and the Genetic Leadership Collaborative.
Dr. Wilcox is a graduate of the University of California, Los Angeles (UCLA) School of Medicine. He completed a residency in pediatrics at UCLA and a genetics fellowship in the UCLA Intercampus Medical Genetics Training Program.
