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Familial Cancer|February 10, 2018
A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC)Priya T Bhola, Cathy Gilpin, Amanda Smith, et al.Familial Cancer|December 25, 2018
Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohortKelly Fulk, Holly LaDuca, Mary Helen Black, et al.Familial Cancer|December 7, 2017
Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgeryRachel Shapira, Erin Turbitt, Lori H Erby, et al.Familial Cancer|October 29, 2018
Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastomaP Vande Perre, A Siegfried, C Corsini, et al.Familial Cancer|November 14, 2016
Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumorCaroline Goehringer, Christian Sutter, Matthias Kloor, et al.Familial Cancer|November 16, 2016
Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancerMakia J Marafie, Mohammed Dashti, Fahd Al-MullaFamilial Cancer|November 17, 2016
Detection of false positive mutations in BRCA gene by next generation sequencingMoushumi Suryavanshi, Dushyant Kumar, Manoj Kumar Panigrahi, et al.Familial Cancer|October 27, 2016
BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancerEstelle Jamard, Bertrand Volard, Audrey Emmanuelle Dugué, et al.Familial Cancer|November 3, 2016
Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in NorwayTrine Levin, Lovise MæhleFamilial Cancer|October 22, 2016
Cystic parathyroid glands in MEN1: A rare entity?Tiziana Cavalli, Francesco Giudici, Gabriella Nesi, et al.Pageof 151