Lynch Syndrome-Associated Extracolonic Tumors Are Rare in Two Extended Families With the Same EPCAM Deletion-Reference-Cited by-同舟云学术

Lynch Syndrome-Associated Extracolonic Tumors Are Rare in Two Extended Families With the Same EPCAM Deletion

Published:2011-10 Issue:10 Volume:106 Page:1829-1836
ISSN:0002-9270
Container-title:American Journal of Gastroenterology
language:en
Short-container-title:

Author:

Lynch Henry T,Riegert-Johnson Douglas L,Snyder Carrie,Lynch Jane F,Hagenkord Jill,Boland Richard C,Rhees Jennifer,Thibodeau Stephen N,Boardman Lisa A,Davies Janine,Kuiper Roland P,Hoogerbrugge Nicoline,Ligtenberg Marjolijn J L

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

Link

http://www.nature.com/articles/ajg2011203.pdf

Reference29 articles.

1. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3 exons of TACSTD1.;Ligtenberg;Nat Genet,2009

2. Silencing is not-so golden: a new model for inheritance of Lynch syndrome.;Kobelka;Clin Genet,2009

3. Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.;Kovacs;Hum Mutat,2009

4. Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.;Niessen;Genes Chromosomes Cancer,2009

5. Recurrence and variability of germline EPCAM deletions in Lynch syndrome.;Kuiper;Hum Mutat,2011

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