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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome SequencingCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mouth Abnormalities, Stomatognathic Diseases, Stomatognathic System Abnormalities, cleft lip, cleft lip/palate, lip disorder, mouth disorderRecruitingNot applicable2026-05-13NCT03065686

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OrganizationsLinked trials
Centre Hospitalier Universitaire, Amiens198

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Research sitesCityCountryLinked trials
CHU Amiens PicardieAmiensFrance18