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Familial Cancer|July 12, 2015
Metastatic sympathetic paraganglioma in a patient with loss of the SDHC geneThereasa Rich, Michelle Jackson, Alejandro Roman-Gonzalez, et al.
Familial Cancer|July 17, 2015
Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UKDhivya Chandrasekaran, Usha Menon, Gareth Evans, et al.
Familial Cancer|June 15, 2015
Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysisMaria João Bugalho, Ana Luísa Silva, Rita Domingues
Familial Cancer|December 31, 2017
Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutationJenny von Salomé, Tao Liu, Markku Keihäs, et al.
Familial Cancer|February 22, 2018
Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to declineAnaita Kanga-Parabia, Clara Gaff, Louisa Flander, et al.
Familial Cancer|February 16, 2018
Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate riskAllison H West, Kathleen R Blazer, Jessica Stoll, et al.
Familial Cancer|November 15, 2017
Germline variant in MSX1 identified in a Dutch family with clustering of Barrett's esophagus and esophageal adenocarcinomaA M J van Nistelrooij, R van Marion, W F J van Ijcken, et al.
Familial Cancer|February 24, 2007
Recurrent idiopathic pancreatitis in familial adenomatous polyposis: report of a case-series and review of the literatureAura A J van Esch, Joost P H Drenth, Rene H M te Morsche, et al.
Familial Cancer|February 27, 2007
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutationAngela Arnold, Stewart Payne, Samantha Fisher, et al.
Familial Cancer|March 3, 2007
Founder mutations in early-onset, familial and bilateral breast cancer patients from RussiaAnna P Sokolenko, Maxim E Rozanov, Natalia V Mitiushkina, et al.
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