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Orofaciodigital Syndromes - 3 Studies Found

Status Study
Completed Study Name: Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene
Condition: Orofaciodigital Syndromes
Date: 2013-10-08
Interventions: Biological: Sampling of blood
Active, not recruiting Study Name: Clinical and Molecular Investigations Into Ciliopathies
Condition:
  • Autosomal Recessive Polycystic Kidney Disease
  • Congenital Hepatic Fibrosis
  • Hepato/Renal Fibrocystic Disease
  • Autosomal Recessive Polycystic Kidney Disease
  • Date: 2011-07-22