Applying CFTR molecular genetics to facilitate the diagnosis of cystic fibrosis through screening

Adv Pediatr. 2002;49:131-90.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Alleles
  • Communication
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / epidemiology
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / classification
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Genetic Counseling
  • Genetic Testing / methods*
  • Genetics, Population
  • Global Health
  • Humans
  • Mutation

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator