Is early identification of asymptomatic infants with 'mild' CFTR genotypes clinically useful?

Acta Paediatr. 2007 Mar;96(3):477-9. doi: 10.1111/j.1651-2227.2007.00142.x.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Child, Preschool
  • Chlorides / analysis
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / physiopathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Female
  • Follow-Up Studies
  • Genetic Carrier Screening
  • Genotype
  • Humans
  • Infant
  • Male
  • Mutation
  • Sweat / chemistry
  • Trypsin

Substances

  • Chlorides
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Trypsin