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Familial Cancer|December 4, 2019
Renal cell carcinoma in young FH mutation carriers: case series and review of the literatureJ A Hol, M C J Jongmans, A S Littooij, et al.Familial Cancer|September 29, 2020
FRAMe: Familial Risk Assessment of Melanoma-a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanomaElizabeth A Holland, Serigne Lo, Blake Kelly, et al.Familial Cancer|August 27, 2022
A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in IrelandTerri Patricia McVeigh, Karl J Sweeney, Donal J Brennan, et al.Familial Cancer|January 4, 2022
BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratoriesHenrikke N Hovland, Rafal Al-Adhami, Sarah Louise Ariansen, et al.Familial Cancer|October 19, 2022
Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMOTrevor L Hoffman, Hilary Kershberg, John Goff, et al.Familial Cancer|April 17, 2019
Implication of DNA repair genes in Lynch-like syndromeRosa M Xicola, Julia R Clark, Timothy Carroll, et al.Familial Cancer|April 17, 2019
Hereditary gastric cancer: what's new? Update 2013-2018Rachel S van der Post, Carla Oliveira, Parry Guilford, et al.Familial Cancer|September 26, 2018
Electronically ascertained extended pedigrees in breast cancer genetic counselingV Stefansdottir, H Skirton, O Th Johannsson, et al.Familial Cancer|June 17, 2019
Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriersE Christodoulou, M Visser, T P Potjer, et al.Familial Cancer|June 24, 2017
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencingMasood Alqahtani, Caitlin Edwards, Natasha Buzzacott, et al.Pageof 152