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
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- Universitätskrankenhaus Hamburg-Eppendorf Hamburg, Germany