We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMSH2 genomic deletions are a frequent cause of HNPCC.AuthorsWijnen, J; van der Klift, H; Vasen, H; Khan, P M; Menko, F; Tops, C; Meijers Heijboer, H; Lindhout, D; Møller, P; Fodde, RPublicationNature genetics, 1998, Vol 20, Issue 4, p326ISSN1061-4036Publication typeResearchDOI10.1038/3795