Screening for cystic fibrosis: use of ΔF508 mutation
- 14 April 1990
- journal article
- Published by Elsevier in The Lancet
- Vol. 335 (8694) , 925-926
- https://doi.org/10.1016/0140-6736(90)90534-c
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Mutation Analysis for Heterozygote Detection and the Prenatal Diagnosis of Cystic FibrosisNew England Journal of Medicine, 1990
- Screening for Cystic FibrosisNew England Journal of Medicine, 1990
- ΔF508 GENE DELETION IN CYSTIC FIBROSIS IN SOUTHERN EUROPEThe Lancet, 1989
- FREQUENCY OF ΔF508 MUTATION ON CYSTIC FIBROSIS CHROMOSOMES IN UKThe Lancet, 1989
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Survival and clinical outcome in patients with cystic fibrosis, with or without neonatal screeningThe Journal of Pediatrics, 1989
- Neonatal screening for cystic fibrosis.Archives of Disease in Childhood, 1988
- REDUCED MORBIDITY IN PATIENTS WITH CYSTIC FIBROSIS DETECTED BY NEONATAL SCREENINGThe Lancet, 1985