Surgical treatment of hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics (clinical),Oncology,Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10689-013-9626-y.pdf
Reference34 articles.
1. Vasen HF, Moslein G, Alonso A et al (2007) Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). J Med Genet 44(6):353–362. doi: 10.1136/jmg.2007.048991
2. Bonadona V, Bonaiti B, Olschwang S et al (2011) Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA 305(22):2304–2310. doi: 10.1001/jama.2011.743
3. Baglietto L, Lindor NM, Dowty JG et al (2010) Risks of Lynch syndrome cancers for MSH6 mutation carriers. J Natl Cancer Inst 102(3):193–201. doi: 10.1093/jnci/djp473
4. Fitzgibbons RJ Jr, Lynch HT, Stanislav GV et al (1987) Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II). Ann Surg 206(3):289–295
5. Vasen HF, Mecklin JP, Khan PM, Lynch HT (1991) The International collaborative group on hereditary non-polyposis colorectal cancer (ICG-HNPCC). Dis Colon Rectum 34(5):424–425
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