Cystic Fibrosis Mutations in Heterozygous Newborns with Hypertrypsinemia and Low Sweat Chloride
- 1 January 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (1) , 303-304
- https://doi.org/10.1086/302212
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Abnormal frequency of ΔF508 mutation in neonatal transitory hypertrypsinaemiaThe Lancet, 1991