MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations

By Giraldo Alejandro   Gómez Andrea   Salguero Gustavo   García Herbert   Aristizábal Fabio   Gutiérrez Óscar   Ángel Luis   Padrón Jorge   Martínez Carlos   Martínez Humberto   Malaver Omar   Flórez Luis   Barvo Rosa  

Familial Cancer, Vol. 4, Iss. 4, 2005-11 ,pp. : 285-290

Springer Publishing Company

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Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome

By Rahner Nils   Friedrichs Nicolaus   Wehner Maria   Steinke Verena   Aretz Stefan   Friedl Waltraut   Buettner Reinhard   Mangold Elisabeth   Propping Peter   Walldorf Constanze  

Acta Oncologica, Vol. 46, Iss. 6, 2007-01 ,pp. : 763-769

Informa Healthcare

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Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH

By Akrami Seyed   Dunlop Malcolm   Farrington Susan   Frayling Ian   MacDonald Fiona   Harvey John   Armour John  

Familial Cancer, Vol. 4, Iss. 2, 2005-06 ,pp. : 145-149

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A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene

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Familial Cancer, Vol. 6, Iss. 1, 2007-03 ,pp. : 141-145

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An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation

By Arnold Angela   Payne Stewart   Fisher Samantha   Fricker Diane   Soloway Judith   White Susan   Novelli Marco   MacDonald Kylie   Mackay James   Groves Richard   Canham Natalie  

Familial Cancer, Vol. 6, Iss. 3, 2007-09 ,pp. : 317-321

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