Genotype-phenotype correlation in five cystic fibrosis patients homozygous for the 621 + 1G-->T mutation

J Med Genet. 1997 Sep;34(9):788-9. doi: 10.1136/jmg.34.9.788.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Cystic Fibrosis / etiology
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis / therapy
  • Female
  • Homozygote*
  • Humans
  • Male
  • Mutation*
  • Phenotype