Clinical trial
Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene
NCT01962129 is registered in ClinicalTrials.gov with Centre Hospitalier Universitaire Dijon as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene
- Lead sponsor
- Centre Hospitalier Universitaire Dijon
- Phase
- Observational
- Overall status
- Unknown status
- Start date
- June 30, 2011
- Completion date
- Not reported
- Enrollment
- 133 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.