| Literature DB >> 7911698 |
A E Hughes1, A M Shearman, J L Weber, R J Barr, R G Wallace, P H Osterberg, N C Nevin, R A Mollan.
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.Entities:
Mesh:
Year: 1994 PMID: 7911698 DOI: 10.1093/hmg/3.2.359
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150