NovelMLH1andMSH2germline mutations in the first HNPCC families identified in Slovakia-Reference-Cited by-同舟云学术

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NovelMLH1andMSH2germline mutations in the first HNPCC families identified in Slovakia

Published:2003-03-19 Issue:4 Volume:21 Page:449-449
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bartosova Zdena,Fridrichova Ivana,Bujalkova Maria,Wolf Brigitte,Ilencikova Denisa,Krizan Peter,Hlavcak Peter,Palaj Julius,Lukac Ludovit,Lukacova Margita,Böör Andrej,Haider Ritva,Jiricny Josef,Nyström-Lahti Minna,Marra Giancarlo

Funder

International Union against Cancer (UICC)

International Cancer Technology Transfer Fellowship (ICRETT) No

Slovak Government Grant Agency VEGA

European Commission (EC)

project of 5th Framework of European Union

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 9 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. MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case;Familial Cancer;2019-11-19

2. Stratification of patients with colorectal cancer without the recorded family history;Oncology Letters;2019-02-06

3. First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome;Familial Cancer;2016-07-28

4. Prevalence of Pathological Germline Mutations of hMLH1 and hMSH2 Genes in Colorectal Cancer;PLoS ONE;2013-03-19

5. Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers;BMC Cancer;2009-11-20

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