NCT00004770
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
- Locations
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Not specified
Clinical trial condition
Explore clinical trials studying Rare Diseases. Study availability and eligibility vary by location and protocol.
NCT00004770
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NCT00004284
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NCT00004649
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NCT00005892
NCT00004804
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NCT00004791
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NCT00004670
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NCT00004288
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NCT00004454
NCT00004760
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