Completed
Estimation of the Carrier Frequency and Incidence of Smith-Lemli-Opitz Syndrome in African Americans
NCT00017732
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
- Locations
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- National Institute of Child Health and Human Development (NICHD) Bethesda, Maryland, United States