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CLINICAL_TRIALS research · 2013-10-14

Clinical Trial Update: Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene

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Summary

Clinical trial update focusing on clinical and molecular characterization of Orofaciodigital syndromes and other phenotypes caused by OFD1 mutations.

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Diseases / indications

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Sponsor: Centre Hospitalier Universitaire Dijon | Conditions: Orofaciodigital Syndromes | Status: UNKNOWN