Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C → T mutation
- 3 July 1993
- journal article
- Published by Elsevier in The Lancet
- Vol. 342 (8862) , 25-26
- https://doi.org/10.1016/0140-6736(93)91885-p
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Cystic Fibrosis Gene Mutation in Two Sisters with Mild Disease and Normal Sweat Electrolyte LevelsNew England Journal of Medicine, 1991
- The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF508)New England Journal of Medicine, 1990
- Linked marker haplotypes and the $Delta;F508 mutation in adults with mild pulmonary disease and cystic fibrosisThe Lancet, 1990
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA MarkerScience, 1985
- A TEST FOR CONCENTRATION OF ELECTROLYTES IN SWEAT IN CYSTIC FIBROSIS OF THE PANCREAS UTILIZING PILOCARPINE BY IONTOPHORESISPediatrics, 1959