作者
Minna Nyström-Lahti, Ramon Parsons, Pertti Sistonen, Lea Pylkkänen, Lauri A Aaltonen, Fredrick S Leach, Stanley R Hamilton, Patrice Watson, Earlene Bronson, Ramon Fusaro, Jennifer Cavalieri, Jane Lynch, Stephen Lanspa, Tom Smyrk, Patrick Lynch, Thomas Drouhard, Kenneth W Kinzler, Bert Vogelstein, Henry T Lynch, Albert De La Chapelle, Päivi Peltomäki
发表日期
1994/10
期刊
American journal of human genetics
卷号
55
期号
4
页码范围
659
出版商
Elsevier
简介
Two susceptibility loci for hereditary nonpolyposis colo-rectal cancer (HNPCC) have been identified, and each contains a mismatch repair gene: MSH2 on chromosome 2p and MLH1 on chromosome 3p. We studied the involvement of these loci in 13 large HNPCC kindreds originating from three different continents. Six families showed close linkage to the 2p locus, and a heritable mutation of the MSH2 gene was subsequently found in four. The 2p-linked kindreds included a family characterized by the lack of extracolonic manifestations (Lynch I syndrome), as well as two families with cutaneous manifestations typical of the Muir-Torre syndrome. Four families showed evidence for linkage to the 3p locus, and a heritable mutation of the MLH1 gene was later detected in three. One 3p-linked kindred was of Amerindian origin. Of the remaining three families studied for linkage, one showed lod scores compatible with …
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