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NCT05047354
- Conditions
- Abnormalities, Multiple, CHILD Syndrome, Congenital Abnormalities, +14 more
- Locations
-
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
Completed
Study of Smith-Lemli-Opitz Syndrome
NCT00001721
- Conditions
- Abnormalities, Multiple, Cleft Palate, Congenital Abnormalities, +20 more
- Locations
-
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
NCT05642221
- Conditions
- Abnormalities, Multiple, Brain Diseases, Brain Diseases, Metabolic, +33 more
- Locations
-
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
Completed
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
-
- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
NCT03720990
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
- Locations
-
- Colorado Children's Hospital Aurora, Colorado, United States
- University of Nebraska Medical Center Omaha, Nebraska, United States
NCT00965068
- Conditions
- Abnormalities, Multiple, Asperger Disorder, Asperger Syndrome, +18 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT00272844
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
- Locations
-
- Children's Hospital Boston Boston, Massachusetts, United States
NCT00114634
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT00064792
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
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
-
- National Institute of Child Health and Human Development (NICHD) Bethesda, Maryland, United States
NCT00070850
- Conditions
- Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Foundation for Blood Research Scarborough, Maine, United States
Active, Not Recruiting
Early Check: Expanded Screening in Newborns
NCT03655223
- Conditions
- 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
- Locations
-
- RTI International Research Triangle Park, North Carolina, United States