Frequency of intron 8 CFTR polythymidine sequence variant in neonatal blood specimens.
- 1 November 1997
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 350 (9088) , 1368-1369
- https://doi.org/10.1016/s0140-6736(05)65140-9
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.Journal of Medical Genetics, 1997
- A mutation in CFTR produces different phenotypes depending on chromosomal backgroundNature Genetics, 1993
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989