Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.
Menéndez, M.; Castellví-Bel, S.; Pineda, M.; de Cid, R.; Muñoz, J.; González, S.; Teulé, À.; Balaguer, F.; Ramón y Cajal, T.; Reñé, Josep M.; Blanco, I.; Castells, A.; Capellà, G.; Clinical Genetics, 2010, vol. 78, issue 2, p 186, ISSN 00099163. ISBN 13990004.

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