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Familial Cancer|December 14, 2006
A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-ItalyFrancesca Bianchi, Eva Galizia, Emilio Porfiri, et al.Familial Cancer|December 13, 2006
Study comparing two types of screening provision for people with von Hippel-Lindau diseaseLindsay Fraser, Sally Watts, Anna Cargill, et al.Familial Cancer|December 13, 2006
An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patientsCatherine F Li, Robert Y Wei, Frank Baliko, et al.Familial Cancer|July 20, 2007
BRCA1/2 mutation analysis in male breast cancer families from North West EnglandD G R Evans, Mike Bulman, Karen Young, et al.Familial Cancer|July 31, 2007
A novel MSH2 germline mutation in a Druze HNPCC familyJamal Zidan, Renée C Niessen, Yael Laitman, et al.Familial Cancer|October 20, 2006
A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 geneM Vernez, P Hutter, C Monnerat, et al.Familial Cancer|January 12, 2007
Identification of a founder BRCA2 mutation in Sardinian breast cancer familiesMaria Monne, Giovanna Piras, Patrizia Fancello, et al.Familial Cancer|May 24, 2007
Prognostic value of BRCA1 mutations in familial breast cancer patients affected by a second primary cancerPavel Elsakov, Juozas Kurtinaitis, Valerij OstapenkoFamilial Cancer|May 24, 2007
Competences, education and support for new roles in cancer genetics services: outcomes from the cancer genetics pilot projectsCatherine Bennett, Hilary Burton, Peter FarndonPageof 152