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 PM; Menko F; Tops C; Meijers Heijboer H; Lindhout D; Møller P; Fodde RPublicationNature genetics, 1998, Vol 20, Issue 4, p326ISSN1061-4036Publication typearticleDOI10.1038/3795