Atypical cystic fibrosis--diagnostic and management dilemmas

J R Soc Med. 2003;96 Suppl 43(Suppl 43):2-10.
No abstract available

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis / therapy
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Diagnostic Tests, Routine / methods
  • Environment
  • Genotype
  • Humans
  • Male
  • Mutation
  • Phenotype
  • Vas Deferens / abnormalities

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator