Pancreatic function and extended mutation analysis in ΔF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels-Reference-Cited by-同舟云学术

Pancreatic function and extended mutation analysis in ΔF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels

Published:2000-08 Issue:2 Volume:137 Page:214-220
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Massie R.John,Wilcken Bridget,Van Asperen Peter,Dorney Stuart,Gruca Margie,Wiley Veronica,Gaskin Kevin

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference46 articles.

1. Dried blood spot screening for cystic fibrosis in the newborn;Crossley;Lancet,1979

2. Newborn screening for cystic fibrosis: its evolution and a review of the current situation;Wilcken;Screening,1993

3. Neonatal screening for cystic fibrosis: a comparison of two strategies for case detection in 1.2 million babies;Wilcken;J Pediatr,1995

4. Abnormal frequency of DF508 mutation in neonatal transitory hypertrypsineamia;Laroche;Lancet,1991

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