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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon SyndromeChopra-Amiel-Gordon syndrome, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, disease, hereditary disease, syndromic diseaseRecruitingNot stated2026-02-17NCT05528744