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Familial Cancer|June 4, 2016
An investigation of the factors effecting high-risk individuals' decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC)Nina Hallowell, Shirlene Badger, Sue Richardson, et al.Familial Cancer|September 23, 2017
Evaluation of an online family history tool for identifying hereditary and familial colorectal cancerF G J Kallenberg, C M Aalfs, F O The, et al.Familial Cancer|September 18, 2017
Mutations in context: implications of BRCA testing in diverse populationsGabriela E S Felix, Yonglan Zheng, Olufunmilayo I OlopadeFamilial Cancer|August 31, 2017
Cancer patients' intentions towards receiving unsolicited genetic information obtained using next-generation sequencingRhodé M Bijlsma, Hester Wessels, Roel H P Wouters, et al.Familial Cancer|September 14, 2017
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a reviewJulian Daniell, John-Paul Plazzer, Anuradha Perera, et al.Familial Cancer|March 28, 2016
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutationAurélia Nguyen, Gaelle Bougeard, Meriam Koob, et al.Familial Cancer|March 28, 2016
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiencyMaureen E Mork, Ester Borras, Melissa W Taggart, et al.Familial Cancer|February 20, 2016
Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneityHenry T Lynch, Trudy G ShawFamilial Cancer|June 24, 2018
Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variantMaria De Bonis, Angelo Minucci, Giovanni Luca Scaglione, et al.Familial Cancer|January 17, 2017
Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controlsSibel Saya, Emma Killick, Sarah Thomas, et al.Pageof 151