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Familial Cancer|July 7, 2011
Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumorsWai Kwan Siu, Chun Yiu Law, Ching Wan Lam, et al.
Familial Cancer|December 1, 2011
Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndromeVictoria M Raymond, Casey M Herron, Thomas J Giordano, et al.
Familial Cancer|December 14, 2011
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German familiesS M Schneegans, A Rosenberger, U Engel, et al.
Familial Cancer|May 9, 2012
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndromeGiovanni Ponti, Lorenza Pastorino, Annamaria Pollio, et al.
Familial Cancer|February 22, 2012
Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in SingaporeVivian Wei Wang, Poh Koon Koh, Wai Leng Chow, et al.
Familial Cancer|October 22, 2011
Implications for cancer genetics practice of pro-actively assessing family history in a General Practice cohort in North West LondonKelly Kohut, Lucia D'Mello, Elizabeth K Bancroft, et al.
Familial Cancer|September 9, 2011
Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patientsSomayeh Shahmoradi, Ali Bidmeshkipour, Ahmad Salamian, et al.
Familial Cancer|March 8, 2012
Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer casesIzabela Brozek, Magdalena Ratajska, Magdalena Piatkowska, et al.
Familial Cancer|February 8, 2012
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patientsMuhammad U Rashid, Sidra Gull, Kashif Asghar, et al.
Familial Cancer|February 8, 2012
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist's initiativeK M Landsbergen, J B Prins, H G Brunner, et al.
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