MSH2 genomic deletions are a frequent cause of HNPCC

J (Juul) van Wijnen, H van der Klift, H Vasen, P Meera Khan, FH Menko, C Tops, EJ Meijers-Heijboer, D (Dick) Lindhout, P Moller, R Fodde

Research output: Contribution to journalArticleAcademicpeer-review

194 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)326-328
Number of pages3
JournalNature Genetics
Volume20
Publication statusPublished - 1998

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