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Familial Cancer|March 11, 2015
Genetic screening in patients with Retinoblastoma in IsraelMichal Sagi, Avishag Frenkel, Avital Eilat, et al.Familial Cancer|August 18, 2020
Clinical phenotypes combined with saturation genome editing identifying the pathogenicity of BRCA1 variants of uncertain significance in breast cancerQiting Wan, Li Hu, Tao Ouyang, et al.Familial Cancer|April 3, 2021
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphomaN van Engelen, F van Dijk, E Waanders, et al.Familial Cancer|April 20, 2021
Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblingsIoana Fugaru, Catherine Goudie, John-Paul CapolicchioFamilial Cancer|April 15, 2021
"I wish that there was more info": characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variantsKathryn G Reyes, Cheyla Clark, Meredith Gerhart, et al.Familial Cancer|March 20, 2013
Surgical treatment of hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome)Miguel A Rodriguez-Bigas, Gabriela MöesleinFamilial Cancer|November 17, 2011
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumorsNils Rahner, Felix F Brockschmidt, Verena Steinke, et al.Familial Cancer|November 17, 2011
Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillanceKarin Y van Spaendonck-Zwarts, Sadhanna Badeloe, Sjoukje F Oosting, et al.Familial Cancer|November 29, 2011
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patientsSusanne Magnusson, Thomas Wiebe, Ulf Kristoffersson, et al.Familial Cancer|November 29, 2011
A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumoursLyn Schofield, Fabienne Grieu, Jack Goldblatt, et al.Pageof 152