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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic

By Kleibl Zdenek  

Breast Cancer Research and Treatment, Vol. 90, Iss. 2, 2005-03 ,pp. : 165-167

Springer Publishing Company

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Springer Publishing Company

Access to resources Recommend Favorite