Clinical trial
Phenotype and Etiology of Pallister-Hall Syndrome
NCT00001404 · National Human Genome Research Institute (NHGRI), NIH · Completed
Key facts
| NCT number | NCT00001404 |
|---|---|
| Title | Phenotype and Etiology of Pallister-Hall Syndrome |
| Official title | Genetic and Clinical Studies of Congenital Anomaly Syndromes |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Malformations, Multiple Abnormalies, Polydactyly |
| Enrollment | 1,170 |
| Start date | Aug 18, 1994 |
| Completion | Jan 7, 2016 |
| First posted | Nov 4, 1999 |
| Last update posted | Dec 16, 2019 |
| Countries | Turkey (Türkiye), United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: