Abnormal frequency of delta F508 mutation in neonatal transitory hypertrypsinaemia

Lancet. 1991 Jan 5;337(8732):55. doi: 10.1016/0140-6736(91)93377-l.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Cystic Fibrosis / blood
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics*
  • Genetic Carrier Screening
  • Humans
  • Infant, Newborn
  • Mutation / genetics*
  • Trypsin / blood*

Substances

  • Trypsin