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Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening
OBJECTIVE: To determine the pancreatic phenotype of infants with cystic fibrosis (CF) diagnosed in the first week of life by a combined immunoreactive trypsin/mutation screening program. DESIGN: A prospective evaluation of pancreatic function in infants with CF at the time of neonatal diagnosis and...
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Main Authors: | , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BMJ Group
2007
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2083233/ https://ncbi.nlm.nih.gov/pubmed/17449517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.2006.107581 |
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