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

Springer Publishing Company

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A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy

By Bianchi Francesca   Galizia Eva   Porfiri Emilio   Belvederesi Laura   Catalani Romina   Loretelli Cristian   Bracci Raffaella   Bearzi Italo   Turchi Chiara   Viel Alessandra   Cellerino Riccardo  

Familial Cancer, Vol. 6, Iss. 1, 2007-03 ,pp. : 97-102

Springer Publishing Company

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Muir-Torre syndrome – an uncommon localization of sebaceous carcinomas following irradiation

By Becker-Schiebe Martina   Hannig Horst   Hoffmann Wolfgang   Donhuijsen Konrad  

Acta Oncologica, Vol. 51, Iss. 2, 2012-02 ,pp. : 265-268

Informa Healthcare

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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

Springer Publishing Company

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The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome

By Stuckless Susan   Parfrey Patrick   Woods Michael   Cox Janet   Fitzgerald G.   Green Jane   Green Roger  

Familial Cancer, Vol. 6, Iss. 1, 2007-03 ,pp. : 1-12

Springer Publishing Company

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