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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Diagnostic Value of Exome/ Genome Sequencing, Conventional Methods in Rare Diseases and Familial Tumor SyndromesDisease Attributes, Genetic Risk Score, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, disease susceptibility, inherited disease susceptibilityRecruitingNot stated2026-05-04NCT04731857

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OrganizationsLinked trials
University Hospital Tuebingen123

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Research sitesCityCountryLinked trials
University Hospital TübingenTübingenGermany14