Linkage Disequilibrium and Haplotype Studies of Chromosome 8p 11.1-21.1 Markers and Werner Syndrome

Werner syndrome (WS) is an autosomal recessive disorder, characterized as a progeroid syndrome, previously mapped to the 8p 11.1-21.1 region. Because WS is so rare, and because many patients are from consanguineous marriages, fine localization of the gene by traditional meiotic mapping methods is un...

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Detalhes bibliográficos
Main Authors: Yu, Chang-En, Oshima, Junko, Goddard, Katrina A. B., Miki, Tetsuro, Nakura, Jun, Ogihara, Toshio, Poot, Martin, Hoehn, Holger, Fraccaro, Marco, Piussan, Charles, Martin, George M., Schellenberg, Gerard D., Wijsman, Ellen M.
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918357/
https://ncbi.nlm.nih.gov/pubmed/8037212
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