Clinical trial
Genetic Analysis of Fraser Syndrome and Fryns Syndrome
NCT00032877 · National Human Genome Research Institute (NHGRI), NIH · Completed
Key facts
| NCT number | NCT00032877 |
|---|---|
| Title | Genetic Analysis of Fraser Syndrome and Fryns Syndrome |
| Official title | Molecular Genetic Analysis of Fraser Syndrome and Fryns Syndrome |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Fraser Syndrome, Fryns Syndrome, Chromosomal Abnormalities, Abnormalities, Multiple |
| Enrollment | 400 |
| Start date | Apr 1, 2002 |
| Completion | Feb 1, 2003 |
| First posted | Apr 5, 2002 |
| Last update posted | Mar 4, 2008 |
| 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: