Nonclassic cystic fibrosis: a clinical conundrum

Pediatr Pulmonol. 2003 Jul;36(1):10-2. doi: 10.1002/ppul.10286.
No abstract available

Publication types

  • Comparative Study

MeSH terms

  • Cystic Fibrosis / epidemiology
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Incidence
  • Infant, Newborn
  • Male
  • Mutation
  • Pedigree
  • Phenotype
  • Prognosis
  • Risk Assessment
  • Severity of Illness Index

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator