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Hereditary Cancer in Clinical Practice|March 13, 2010
Some aspects of molecular diagnostics in Lynch syndromeGrzegorz Kurzawski
Hereditary Cancer in Clinical Practice|March 13, 2010
Withdrawal from genetic counselling for cancerEveline Bleiker, Gea Wigbout, Anja van Rens, et al.
Hereditary Cancer in Clinical Practice|March 13, 2010
Update on the cytogenetics and molecular genetics of chordomaLidia Larizza, Pietro Mortini, Paola Riva
Hereditary Cancer in Clinical Practice|March 13, 2010
The Swedish family-cancer database: update, application to colorectal cancer and clinical relevanceKari Hemminki, Charlotta Granström, Bowang Chen
Hereditary Cancer in Clinical Practice|March 13, 2010
Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC PatientsKatie A Ashton, Cliff J Meldrum, Mary L McPhillips, et al.
Hereditary Cancer in Clinical Practice|March 13, 2010
Clinical outcome of hereditary breast cancer in the lithuanian populationPavel Elsakov, Juozas Kurtinaitis, Valerij Ostapenko
Hereditary Cancer in Clinical Practice|March 13, 2010
Case report: familial gastric cancer and chordoma in the same familyWalter Weber, Rodney J Scott
Hereditary Cancer in Clinical Practice|March 13, 2010
Patient perspective on the value of genetic counselling for familial pancreas cancerJennifer E Axilbund, Kieran A Brune, Marcia I Canto, et al.
Hereditary Cancer in Clinical Practice|December 24, 2009
Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical managementDewkoemar Ramsoekh, Anja Wagner, Monique E van Leerdam, et al.
Hereditary Cancer in Clinical Practice|September 8, 2016
Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancerMatilde Pensabene, Caterina Condello, Chiara Carlomagno, et al.
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