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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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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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

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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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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