Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families-Reference-Cited by-同舟云学术

Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families

Published:2012-03-01 Issue:3 Volume:11 Page:519-524
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Tanyi Miklós,Olasz Judit,Tanyi Janos L.,Tóth László,Antal-Szalmás Péter,Bubán Tamás,András Csilla,Urbancsek Hilda,Garami Zoltán,Csuka Orsolya,Damjanovich László

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-012-9515-9.pdf

Reference32 articles.

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3. Loukola A, Eklin K, Laiho P et al (2001) Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC). Cancer Res 61:4545–4549

4. Dieumegard B, Grandjouan S, Sabourin JC et al (2000) Extensive molecular screening for non-polyposis colorectal cancer. Br J Cancer 82:871–880

5. Lynch HT, Jass J, Lynch JF et al (2005) Hereditary colorectal cancer: an updated review. Part II: the lynch syndrome (hereditary nonpoliposis colorectal cancer). Gastroentol Hepatol 1:117–127

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of Novel Pathogenic Sequence Variants of the Mismatch Repair Genes During Screening for Lynch Syndrome in a Single Centre of Eastern Hungary;Journal of Gastrointestinal Cancer;2020-01-14

2. MLH1 and MSH2 mutation screening in HNPCC families of Hungary – Two new MMR gene mutations;European Journal of Surgical Oncology (EJSO);2014-11

3. Epithelial-mesenchymal transition in colorectal cancer tissue of patients with Lynch syndrome;World Journal of Gastroenterology;2014