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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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Detalhes bibliográficos
Main Authors: Cipolli, Marco, Castellani, Carlo, Wilcken, Bridget, Massie, John, McKay, Karen, Gruca, Margie, Tamanini, Anna, Assael, Maurice Baroukh, Gaskin, Kevin
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
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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