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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Contribution of Optical Genome Mapping (OGM) in the Diagnosis of Multiple Congenital Malformations With or Without Intellectual Disability Without Genetic AbnormalityAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesRecruitingNot applicable2026-01-27NCT07370792

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OrganizationsLinked trials
Céline PEBREL-RICHARD1

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Research sitesCityCountryLinked trials
CHU Clermont-FerrandClermont-FerrandFrance62