The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome-Reference-Cited by-同舟云学术

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The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome

Published:2013-02-27 Issue:2 Volume:12 Page:175-180
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Plazzer J. P.,Sijmons R. H.,Woods M. O.,Peltomäki P.,Thompson B.,Den Dunnen J. T.,Macrae F.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-013-9616-0.pdf

Reference8 articles.

1. Fokkema IF, Taschner PE, Schaafsma GC et al (2011) LOVD v. 2.0: the next generation in gene variant databases. Hum Mutat 32:557–563

2. Peltomäki P, Vasen H (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 113:1146–1158

3. Peltomäki P, Vasen H (2004) Mutations associated with HNPCC predisposition—update of ICG-HNPCC/INSiGHT mutation database. Dis Markers 20:269–276

4. Woods MO, Williams P, Careen A et al (2007) A new variant database for mismatch repair genes associated with Lynch syndrome. Hum Mutat 28:669–673

5. Ou J, Niessen RC, Vonk J et al (2008) A database to support the interpretation of human mismatch repair gene variants. Hum Mutat 29:1337–1341

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