Literature DB >> 18301442

Modifier genes and HNPCC: variable phenotypic expression in HNPCC and the search for modifier genes.

Rodney J Scott.   

Abstract

Mesh：

Year:  2008        PMID： 18301442     DOI： 10.1038/ejhg.2008.46

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN： 1018-4813            Impact factor:   4.246


× No keyword cloud information.
  3 in total

1.  Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers.

Authors:  Ramunas Janavicius; Pavel Elsakov
Journal:  Hered Cancer Clin Pract       Date:  2012-01-10       Impact factor: 2.857

2.  The G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndrome.

Authors:  M Clyne; J Offman; S Shanley; J D Virgo; M Radulovic; Y Wang; A Ardern-Jones; R Eeles; E Hoffmann; V P C C Yu
Journal:  Br J Cancer       Date:  2009-01-13       Impact factor: 7.640

3.  Unusual presentation of Lynch Syndrome.

Authors:  Veronica P C C Yu; Marco Novelli; Stewart J Payne; Sam Fisher; Rebecca A Barnetson; Ian M Frayling; Ann Barrett; David Goudie; Audrey Ardern-Jones; Ros Eeles; Susan Shanley
Journal:  Hered Cancer Clin Pract       Date:  2009-06-03       Impact factor: 2.857
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.