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Familial Cancer|September 4, 2014
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern EuropeNatalia Bogdanova, Alexandr V Togo, Magdalena Ratajska, et al.
Familial Cancer|September 5, 2020
Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working GroupSimone Hettmer, Guillaume Dachy, Guido Seitz, et al.
Familial Cancer|November 9, 2020
Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factorsYael Laitman, Rachel Michaelson-Cohen, Rakefet Chen-Shtoyerman, et al.
Familial Cancer|September 19, 2020
Quantitative evaluation of MSI testing using NGS detects the imperceptible microsatellite changed caused by MSH6 deficiencyGou Yamamoto, Takashi Takenoya, Akemi Takahashi, et al.
Familial Cancer|January 11, 2016
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safetyErica Sermijn, Liesbeth Delesie, Ellen Deschepper, et al.
Familial Cancer|February 13, 2016
Evaluation of laboratory perspectives on hereditary cancer panelsJessica Stoll, Scott M Weissman, Nicole Hook, et al.
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