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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Detection of Single Nucleotide Polymorphism (SNP) Rs2235371 of IRF6 Gene in Egyptian Patients with Non-Syndromic Cleft Lip and PalateCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Jaw Abnormalities, Jaw Diseases, Maxillofacial Abnormalities, Mouth Abnormalities, Musculoskeletal Abnormalities, Stomatognathic Diseases, Stomatognathic System Abnormalities, cleft lip, cleft palate, lip disorder, mouth disorder, musculoskeletal system disorderNot yet recruitingNot stated2024-12-12NCT06730880

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OrganizationsLinked trials
Assiut University1477

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