Carrier screening, incidence of cystic fibrosis, and difficult decisions

JAMA. 2009 Dec 16;302(23):2595-6. doi: 10.1001/jama.2009.1865.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Adult
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / epidemiology*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Genetic Carrier Screening*
  • Genetic Testing*
  • Humans
  • Incidence
  • Infant, Newborn
  • Italy
  • Mutation
  • Neonatal Screening

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator