Cystic fibrosis syndrome: a new paradigm for inherited disorders and implications for molecular diagnostics

Clin Chem. 1999 Jul;45(7):929-31.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Electrophoresis / methods
  • Humans
  • Mutation

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator