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Hereditary Cancer in Clinical Practice|December 19, 2013
Mutation spectrum in South American Lynch syndrome familiesMev Dominguez-Valentin, Mef Nilbert, Patrik Wernhoff, et al.Hereditary Cancer in Clinical Practice|April 3, 2009
Large family with both parents affected by distinct BRCA1 mutations: implications for genetic testingAnna P Sokolenko, Dmitry A Voskresenskiy, Aglaya G Iyevleva, et al.Hereditary Cancer in Clinical Practice|April 3, 2009
The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotypeMarielle W G Ruijs, Annegien Broeks, Fred H Menko, et al.Hereditary Cancer in Clinical Practice|May 22, 2010
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancerBente A Talseth-Palmer, Mary McPhillips, Claire Groombridge, et al.Hereditary Cancer in Clinical Practice|April 6, 2010
Surveillance of FAP: a prospective blinded comparison of capsule endoscopy and other GI imaging to detect small bowel polypsPaul Tescher, Finlay A Macrae, Tony Speer, et al.Hereditary Cancer in Clinical Practice|September 4, 2009
Familial multiple myeloma: report on two families and discussion of screening optionsErica H Gerkes, Mirjam M de Jong, Rolf H Sijmons, et al.Hereditary Cancer in Clinical Practice|September 4, 2009
Some molecular and clinical aspects of genetic predisposition to malignant melanoma and tumours of various site of originTadeusz DebniakHereditary Cancer in Clinical Practice|September 4, 2009
Selected aspects of inherited susceptibility to prostate cancer and tumours of different site of originCezary CybulskiHereditary Cancer in Clinical Practice|September 4, 2009
Recurrent APC gene mutations in Polish FAP familiesAndrzej Pławski, Marta Podralska, Ryszard SłomskiHereditary Cancer in Clinical Practice|September 4, 2009
Base excision repair and the role of MUTYHCarla Kairupan, Rodney J ScottPageof 48