Diagnosing cystic fibrosis: blood, sweat, and tears

Arch Dis Child. 1997 Feb;76(2):85-8. doi: 10.1136/adc.76.2.85.
No abstract available

Publication types

  • Review

MeSH terms

  • Child
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Genotype
  • Humans
  • Mutation
  • Sweat / chemistry*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator