| Literature DB >> 16773566 |
Anne-Louise Leutenegger1, Audrey Labalme, Emmanuelle Genin, Annick Toutain, Elisabeth Steichen, Francoise Clerget-Darpoux, Patrick Edery.
Abstract
The use of inbred patients whose exact genealogy may not be available is of primary interest in mapping genes involved in rare recessive diseases. We show here that this can be achieved by estimating inbreeding coefficients from the patients' genomic information and using these estimates to perform homozygosity mapping. We show the interest of the approach by mapping a gene for Taybi-Linder syndrome to chromosome 2q, with the use of a key patient with no genealogical information.Entities:
Mesh:
Year: 2006 PMID: 16773566 PMCID: PMC1474127 DOI: 10.1086/504640
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025