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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive RisksAbnormalities, Multiple, Beckwith-Wiedemann syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, chromosomal disorder, hereditary diseaseRecruitingNot applicable2025-05-02NCT06346418

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Research sitesCityCountryLinked trials
Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoMilanItaly44
Istituto Auxologico ItalianoMilanItaly4