Recruiting Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168 Conditions 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more Locations Sanford Health — Sioux Falls, South Dakota, United States Online Patient Enrollment System — Sydney, Australia View Trial Details
Completed Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases NCT01252901 Conditions Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +35 more Locations Universitätskrankenhaus Hamburg-Eppendorf — Hamburg, Germany View Trial Details
