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

By Vernez M.   Hutter P.   Monnerat C.   Halkic N.   Gugerli O.   Bouzourene H.  

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

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The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family

By Puijenbroek Marjo   Nielsen Maartje   Reinards Tjitske   Weiss Marjan   Wagner Anja   Hendriks Yvonne   Vasen Hans   Tops Carli   Wijnen Juul   Wezel Tom   Hes Frederik   Morreau Hans  

Familial Cancer, Vol. 6, Iss. 1, 2007-03 ,pp. : 43-51

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Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I

By Toledano Helen   Goldberg Yael   Kedar-Barnes Inbal   Baris Hagit   Porat Rinnat   Shochat Chen   Bercovich Dani   Pikarsky Eli   Lerer Israela   Yaniv Isaac   Abeliovich Dvorah   Peretz Tamar  

Familial Cancer, Vol. 8, Iss. 3, 2009-09 ,pp. : 187-194

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A Novel Exon Duplication Event Leading to a Truncating Germ-line Mutation of the APC Gene in a Familial Adenomatous Polyposis Family

By McCart Amy   Latchford Andrew   Volikos Emmanouil   Rowan Andrew   Tomlinson Ian   Silver Andrew  

Familial Cancer, Vol. 5, Iss. 2, 2006-06 ,pp. : 205-208

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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

Springer Publishing Company

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