Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation-Reference-Cited by-同舟云学术

Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation

Published:2011-02-01 Issue:2 Volume:10 Page:285-295
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Lastella Patrizia,Patruno Margherita,Forte Giovanna,Montanaro Alba,Di Gregorio Carmela,Sabbà Carlo,Suppressa Patrizia,Piepoli Adalgisa,Panza Anna,Andriulli Angelo,Resta Nicoletta,Stella Alessandro

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-011-9419-0.pdf

Reference52 articles.

1. Hampel H, Frankel Wl, Martin E et al (2005) Screening for the lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 352:1851–1860

2. Lynch H, de la Chapelle A (2003) Hereditary colorectal cancer. N Engl J Med 348(10):919–932

3. Peltomäki P, Vasen HF (1997) Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on hereditary nonpolyposis colorectal cancer. Gastroenterology 11:1146–1158

4. Lagerstedt Robinson K, Liu T, Vandrovcova J et al (2007) Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. J Natl Cancer Inst 99(4):291–299

5. Mueller J, Gazzoli I, Bandipalliam P, Garber JE, Syngal S, Kolodner RD (2009) Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases. Cancer Res 69:7053–7061

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2. Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome;The International Journal of Biological Markers;2018-04-24

3. A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America;BMC Cancer;2017-09-05

4. Molecular testing for Lynch syndrome in people with colorectal cancer: systematic reviews and economic evaluation;Health Technology Assessment;2017-09

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