Fellowship · Philadelphia, PA
Sponsored by Children's Hospital of Philadelphia
Program Director, Medical Biochemical Genetics Fellowship
Clinical biochemical genetics physician, Associate Professor of Pediatrics at Children's Hospital of Philadelphia
Director, Section of Biochemical Genetics
Clinical biochemical genetics physician, Professor of Pediatrics (Human Genetics) at the Children's Hospital of Philadelphia at Children's Hospital of Philadelphia
Chief of the Division of Genetic and Genomic Medicine
Clinical genetics and genomics physician at The Association of CHRMC and University Physicians
Faculty
Clinical biochemical genetics physician, Chair at University of Pennsylvania Health System
Pediatrics, Human genetics, Glycosylation Metabolic Disease
Faculty
Pediatric medicine physician, Assistant Professor of Clinical Pediatrics (Human Genetics) at University of Pennsylvania Health System
Co-Director of Metabolic and Advanced Diagnostics
Adjunct Associate Professor of Pathology and Laboratory Medicine at University of Pennsylvania Health System
Faculty
Clinical genetics and genomics physician, Associate Professor of Pediatrics (Human Genetics) at University of Pennsylvania Health System
We study rare genetic disorders of the heart and brain both to further our understanding of basic biology and to develop new therapies for our patients., Genetics, inborn errors of metabolism, neurogenetics, molecular therapeutics, gene therapy
Assistant Professor of Pathology and Laboratory Medicine
Medical genetics / clinical biochemical genetics physician, Assistant Professor of Pathology and Laboratory Medicine at the Children's Hospital of Philadelphia at University of Pennsylvania Health System