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

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Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families

By Dovrat Shiri   Figer Arie   Fidder Herma   Neophytou Pavlos   Fireman Zvi   Geva Ravit   Zidan Jamal   Flex Dov   Meir Shimon   Friedman Eitan  

Familial Cancer, Vol. 4, Iss. 4, 2005-11 ,pp. : 291-294

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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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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

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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