William R. Wilcox, MD, PhD
Director, Metabolic Disorders Clinic
Director, Lysosomal Storage Disease Program
Director, Skeletal Dysplasia Morphology and Molecular Laboratory
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 Program at Cedars-Sinai and a Professor in the Medical Genetics Fellowship Program.
Dr. Wilcox is board certified in clinical genetics, clinical biochemical genetics and clinical molecular genetics. His current research interests include treatment of lysosomal storage diseases; the clinical definition, morphology, pathophysiology and treatment of human dwarfing conditions (skeletal dysplasias); and genetic defects in the Marinesco-Sjögren syndrome. He is on the advisory board of the Fabry Disease Registry and chairs the American College of Medical Genetics Therapeutics Committee.
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.
