Uptake of genetic testing by the children of Lynch syndrome variant carriers across three generations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg2017132.pdf
Reference30 articles.
1. Møller P, Seppälä T, Bernstein I et al: Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. Gut 2017; 66: 464–472.
2. Hampel H, la Chapelle de A : The search for unaffected individuals with Lynch syndrome: do the ends justify the means? Cancer Prev Res (Phila) 2011; 4: 1–5.
3. Vasen HFA, Blanco I, Aktán-Collán K et al: Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut 2013; 62: 812–823.
4. Giardiello FM, Allen JI, Axilbund JE et al: Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer. Am J Gastroenterol 2014; 109: 1159–1179.
5. Stoffel EM, Mangu PB, Gruber SB et al: Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline Endorsement of the Familial Risk-Colorectal Cancer: European Society for Medical Oncology Clinical Practice Guidelines. J Clin Oncol 2014; 11: e437–e441.
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1. National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families—The Danish Model;Cancers;2024-04-20
2. Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model;PLOS ONE;2022-12-22
3. Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis;Journal of Clinical Oncology;2022-12-10
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