Optimal DNA tier for the IRT/DNA algorithm determined by CFTR mutation results over 14years of newborn screening

Author:

Baker Mei W.,Groose Molly,Hoffman Gary,Rock Michael,Levy Hara,Farrell Philip M.

Funder

Cystic Fibrosis Foundation

National Institutes of Health

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference23 articles.

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

2. Systematic neonatal screening for mucoviscidosis using an immunoreactive trypsin blood assay. Evaluation of 80,000 tests;Travert;Arch Fr Pédiatr,1983

3. Efficacy of statewide neonatal screening for cystic fibrosis by assay of trypsinogen concentrations;Hammond;N Engl J Med,1991

4. Newborn screening for cystic fibrosis is complicated by the age-related decline in immunoreactive trypsinogen levels;Rock;Pediatrics,1990

5. The application of DNA analysis in a population screening program for neonatal diagnosis of cystic fibrosis: comparison of screening protocols;Gregg;Am J Hum Genet,1993

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