MSH2 genomic deletions are a frequent cause of HNPCC

descriptionPublicationkeyboard_double_arrow_right Article , Other literature type 01 Dec 1998 Netherlands English Publisher:Springer Science and Business Media LLCJournal:Nature Genetics, volume 20, pages 326-328 (issn: 1061-4036, eissn: 1546-1718,

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Authors: Wijnen, J.; van der Klift, H.; Vasen, H.; Khan, P. M.; Menko, F.; Tops, C.; Meijers Heijboer, H.; +3 Authors

doi: 10.1038/3795

pmid: 9843200

MSH2 genomic deletions are a frequent cause of HNPCC

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Country

Netherlands

Related Organizations

Erasmus University Rotterdam
Netherlands
Amsterdam UMC
Netherlands
Leiden University Medical Center
Netherlands

Keywords

Base Sequence, Base Pair Mismatch, Exons, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA-Binding Proteins, MutS Homolog 2 Protein, Proto-Oncogene Proteins, Humans, Genetic Predisposition to Disease, EMC MGC-02-96-01, Gene Deletion

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