A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes

J Med Genet. 1989 Aug;26(8):490-3. doi: 10.1136/jmg.26.8.490.

Abstract

From analysis of DNA polymorphisms in a panel of 455 subjects from 25 families with facioscapulohumeral (Landouzy-Déjérine) disease, we have found no evidence for close linkage of the disease at 24 different genetic loci, including one from a candidate chromosomal region. Added to previous data, our results provide direction for future collaborative linkage studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Chromosomes, Human, Pair 18
  • DNA Probes
  • Female
  • Genetic Linkage*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Muscular Dystrophies / genetics*
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA Probes