Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients

Heleen M. van der Klift*, Carli M. J. Tops, Elsa C. Bik, Merel W. Boogaard, Anne-Marijke Borgstein, Kerstin B. M. Hansson, Margreet G. E. M. Ausems, Encarna Gomez Garcia, Andrew Green, Frederik J. Hes, Louise Izatt, Liselotte P. van Hest, Angel M. Alonso, Annette H. J. T. Vriends, Anja Wagner, Wendy A. G. van Zelst-Stams, Hans F. A. Vasen, Hans Morreau, Peter Devilee, Juul T. Wijnen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

46 Citations (Web of Science)
Original languageEnglish
Pages (from-to)578-587
JournalHuman Mutation
Issue number5
Publication statusPublished - May 2010


  • PMS2
  • PMS2CL
  • pseudogene
  • Lynch syndrome

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