CompletedNCT03139903
The Primordial Dwarfisms: Diagnosis, Identification of the Molecular Basis of Seckel Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II
Studying Microcephalic osteodysplastic primordial dwarfism type II
Last synced from ClinicalTrials.gov
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Report missing dataKey facts
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Principal Investigator
- CORMIER-DAIRE Valérie, PhDMedical Genetics Department and INSERM U781, Necker-Enfants Malades Hospital, 75743 Paris, France
- Enrollment
- 30 enrolled
- Eligibility
- All sexes
- Timeline
- 2010 – 2015
Study locations (1)
- Medical Genetics Department and INSERM U781, Necker-Enfants Malades Hospital, Paris, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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