Cystic fibrosis in Greece: typing with DNA probes and identification of the common molecular defect

Hum Genet. 1990 Sep;85(4):393-4. doi: 10.1007/BF02428270.

Abstract

The relative frequency of the delta F508 mutation in the Greek population is 54.1%; this is similar to that reported in other Southern European populations and contrasts with the considerably higher frequencies encountered in Northern Europe and North America. The low frequency is in agreement with the linkage disequilibrium already reported between cystic fibrosis and haplotype B in this country. In contrast to the common association of pancreatic insufficiency with the homozygous delta F508 genotype, the present study revealed two homozygous children with no evidence of pancreatic failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Deletion
  • Cystic Fibrosis / epidemiology
  • Cystic Fibrosis / genetics*
  • DNA Probes
  • Gene Frequency
  • Greece / epidemiology
  • Humans

Substances

  • DNA Probes