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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of Multilocus Methylation Abnormalities in Subjects With Imprinting DisordersCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, hereditary diseaseNot yet recruitingNot applicable2026-03-27NCT07497477

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OrganizationsLinked trials
Assistance Publique - Hôpitaux de Paris985

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