Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00745.x/fullpdf
Reference33 articles.
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2. Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer;Mangold;Int J Cancer,2005
3. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC);Van Der Klift;Genes Chromosomes Cancer,2005
4. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach;Gille;Br J Cancer,2002
5. Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC;Di Fiore;J Med Genet,2004
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