The faculty and staff in the Division of Medical Genetics provide clinical genetic services at Stanford Children’s Health and Stanford Healthcare including general genetics/dysmorphology and biochemical genetics. In addition, we participate in multi-specialty clinics for craniofacial conditions, Down syndrome, neurogenetics and genetic disorders of the skin. Our educational programs include a two-year residency in Medical Genetics, a combined Pediatrics Medical Genetics Residency, a two year Master’s Program in Human Geneticist Genetic Counseling and a Medical Biochemical Fellowship. The faculty and staff are also involved in the education of medical students as well as residents and fellows from a variety of specialties. Our faculty and staff are involved in a wide variety of research projects, collaborating with researchers at Stanford and worldwide. We participate in ongoing projects in mitochondrial disorders, prenatal genetic screening and diagnosis, autism, the RASopathies, Down syndrome and fetal alcohol syndrome.