Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history.-Reference-Cited by-同舟云学术

Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history.

Published:1993-04-01 Issue:4 Volume:68 Page:464-467
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Green M R,Weaver L T,Heeley A F,Nicholson K,Kuzemko J A,Barton D E,McMahon R,Payne S J,Austin S,Yates J R

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Prospective study of cystic fibrosis in infants identified by screening: natural history and assessment of intervention;Green, M.R.; Nicholson, K.; Heeley, A.F.;Pediatr Pulmonol Suppl,1990

2. Screening for cystic fibrosis by dried blood spot trypsin assay;Heeley, A.F.; Heeley, M.A.; King, D.N.; Kuzemko, J.A.; Walsh, M.P.;Arch Dis Child,1982

3. Improved sweat test method for the diagnosis of cystic fibrosis;Carter, E.P.; Barrett, A.D.; Heeley, A.F.; Kuzemko, J.A.;Arch Dis Child,1984

4. The CF nurse specialist and neonatal screening: child care and research in East Anglia;Nicholson, K.,1992

5. Identification of the cystic fibrosis gene: cloning and characterisation of complementary DNA;Riordan, JR, Rommens; JM, Kerem; B.-S.;Science,1989

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