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Familial Cancer|January 12, 2010
Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndromeChau-To Kwok, Robyn L Ward, Nicholas J Hawkins, et al.
Familial Cancer|May 31, 2018
The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot studyKelly Reumkens, Marly H E Tummers, Joyce J G Gietel-Habets, et al.
Familial Cancer|June 2, 2009
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypesValérie Chaudru, M T Lo, F Lesueur, et al.
Familial Cancer|February 26, 2009
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysisMichael D Walsh, Daniel D Buchanan, Rhiannon Walters, et al.
Familial Cancer|April 29, 2009
CHEK2*1100delC does not contribute to risk to breast cancer among Malay, Chinese and Indians in MalaysiaEswary Thirthagiri, Leng San Cheong, Cheng Har Yip, et al.
Familial Cancer|January 6, 2009
Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician originCatarina Santos, Ana Peixoto, Patrícia Rocha, et al.
Familial Cancer|January 6, 2009
Breast cancer immunohistochemistry can be useful in triage of some HNPCC familiesS Shanley, C Fung, J Milliken, et al.
Familial Cancer|December 23, 2008
Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type IHelen Toledano, Yael Goldberg, Inbal Kedar-Barnes, et al.
Familial Cancer|January 24, 2009
Men in the women's world of hereditary breast and ovarian cancer--a systematic reviewNina Strømsvik, Målfrid Råheim, Nina Oyen, et al.
Familial Cancer|May 8, 2004
BRCA1 testing in breast and/or ovarian cancer families from northeastern France identifies two common mutations with a founder effectDanièle Muller, Catherine Bonaiti-Pellié, Joseph Abecassis, et al.
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