William R. Wilcox, MD, PhD
Director, Metabolic Disorders Clinic
Director, Lysosomal Storage Disease Treatment and Research Center
Director, Skeletal Dysplasia Morphology and Molecular Laboratory
William R. Wilcox, MD, PhD is Director of the Metabolic Disorders Clinic, the Lysosomal Storage Disease Treatment and Research Center, and the Skeletal Dysplasia Morphology and Molecular Laboratory at Cedars-Sinai Medical Center. Dr. Wilcox is also Associate Professor of Pediatrics at University of California, Los Angeles (UCLA) School of Medicine.
Specializing in clinical and metabolic genetics, Dr. Wilcox has conducted several clinical trials on lysosomal storage diseases. His laboratory research focuses on the skeletal dysplasias and the Marinesco-Sjögren syndrome.
Dr. Wilcox is a member of the American Society of Human Genetics, American College of Medical Genetics, American Academy of Pediatrics, Society for Inherited Metabolic Disease and the International Skeletal Dysplasia Society.
Dr. Wilcox received his medical degree and doctorate in molecular biology from UCLA. He completed his internship and residency in pediatrics at UCLA and his fellowship in medical genetics in the UCLA Intercampus Medical Genetics training program.
