Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene
|2||Active, not recruiting||
Clinical and Molecular Investigations Into Ciliopathies
UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
† Study has passed its completion date and status has not been verified in more than two years.