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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical Registry Investigating Bardet-Biedl SyndromeAbnormalities, Multiple, Bardet-Biedl syndrome, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, brain disorder, central nervous system disorder, eye disorder, hereditary disease, hypothalamic disorder, nervous system disorder, retinitis pigmentosaRecruitingNot stated2022-07-19NCT02329210

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OrganizationsLinked trials
Marshfield Clinic Research Foundation2

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Research sitesCityCountryLinked trials
Marshfield Clinic Research FoundationMarshfieldUnited States1