Genetic linkage of familial expansile osteolysis to chromosome 18q

Hum Mol Genet. 1994 Feb;3(2):359-61. doi: 10.1093/hmg/3.2.359.

Abstract

Familial expansile osteolysis is a rare bone dysplasia which is transmitted as an autosomal dominant trait in a large kindred in Northern Ireland. The gene which causes the disease shows tight linkage with several polymorphic markers on chromosome 18q with a maximum lod score of 11.53 at a recombination fraction of 0.00 with D18S64. The gene is flanked by D18S35 and D18S61 and is located at chromosome 18q21.1-q22. Mapping a new locus for a gene involved in regulation of bone metabolism may also have implications in the study of Paget's disease of bone which is a common related bone dysplasia.

Publication types

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

MeSH terms

  • Animals
  • Chromosome Mapping
  • Chromosomes, Human, Pair 18*
  • Female
  • Genes, Dominant*
  • Haplotypes / genetics
  • Humans
  • Lod Score
  • Male
  • Mice
  • Mice, Mutant Strains / genetics
  • Northern Ireland
  • Osteitis Deformans / genetics
  • Osteolysis / genetics*
  • Pedigree
  • Polymorphism, Restriction Fragment Length