NCT00079742
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
- Locations
-
Not specified
Clinical trial condition
Explore clinical trials studying Infant, Newborn, Diseases. Study availability and eligibility vary by location and protocol.
NCT00079742
Not specified
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