MSH2 genomic deletions are a frequent cause of HNPCC [2]

J. Wijnen, H. Van der Klift, H. F.A. Vasen, P. M. Khan, F. Menko, C. Tops, H. M. Heijboer, D. Lindhout, P. Moller, R. Fodde*

*Corresponding author for this work

Research output: Contribution to journalLetterAcademicpeer-review

Original languageEnglish
Pages (from-to)326-328
Number of pages3
JournalNature Genetics
Volume20
Issue number4
DOIs
Publication statusPublished - 1998
Externally publishedYes

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