Making the diagnosis of cystic fibrosis

J Pediatr. 1998 Apr;132(4):563-5. doi: 10.1016/s0022-3476(98)70337-3.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Consensus Development Conferences as Topic
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Humans
  • Membrane Potentials
  • Mutation
  • Nasal Mucosa / physiology
  • Sweat / chemistry

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator