Different molecular mechanisms underlie genomic deletions in theMLH1 Gene-Reference-Cited by-同舟云学术

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Different molecular mechanisms underlie genomic deletions in theMLH1 Gene

Published:2002-10-25 Issue:5 Volume:20 Page:368-374
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Viel Alessandra,Petronzelli Fiorella,Puppa Lara Della,Lucci-Cordisco Emanuela,Fornasarig Mara,Pucciarelli Salvatore,Rovella Valentina,Quaia Michele,de Leon Maurizio Ponz,Boiocchi Mauro,Genuardi Maurizio

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population

2. MLH1 and MSH2 constitutinal mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer

3. Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility

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1. The Contribution of Alu Elements to Mutagenic DNA Double-Strand Break Repair;PLOS Genetics;2015-03-11

3. Alu in Lynch Syndrome: A Danger SINE?;Cancer Prevention Research;2011-10

4. Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome;Journal of Medical Genetics;2011-06-28

5. Alu distribution and mutation types of cancer genes;BMC Genomics;2011-03-23

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