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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Implementation-effectiveness Trial of Mainstreaming of Clinical Genomic Sequencing for Rare Disease in Ontario, CanadaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, hereditary diseaseNot yet recruitingNot stated2026-09-02NCT07799792

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The Hospital for Sick Children162

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