Clinical trial
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene…
NCT00004351 · National Institute of Neurological Disorders and Stroke (NINDS), NIH · Completed
Key facts
| NCT number | NCT00004351 |
|---|---|
| Title | Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes |
| Lead sponsor | National Institute of Neurological Disorders and Stroke (NINDS), NIH |
| Collaborators | Baylor College of Medicine |
| Status | Completed |
| Study type | Observational |
| Conditions | Williams Syndrome, Angelman Syndrome, Prader-Willi Syndrome, Shprintzen Syndrome, Smith-Magenis Syndrome, DiGeorge Syndrome, Chromosome Abnormalities |
| Enrollment | 20 |
| Start date | Sep 1, 1999 |
| First posted | Oct 19, 1999 |
| Last update posted | Jun 24, 2005 |
| Countries | 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.
About ClinicalTrials.gov studies
ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.
Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: