NCT06712095
- Conditions
- BMPR1A Gene Mutation, CDH1 Gene Mutation, CHEK2 Gene Mutation, +28 more
- Locations
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- The Royal Marsden NHS Foundation Trust London, (Select), United Kingdom
Clinical trial condition
Li Fraumeni Syndrome
Explore clinical trials studying Li Fraumeni Syndrome. Study availability and eligibility vary by location and protocol.
2 public trials
1 recruiting study
Li Fraumeni Syndrome trial results
NCT01464086
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Genetic Diseases, Inborn, +6 more
- Locations
-
- Institut Gustave Roussy Villejuif, France