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Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers
- Correspondence to Dr Wenche Sjursen, Department of Pathology and Medical Genetics, Erling Skjalgssons gt 1, St Olavs University Hospital, 7006 Trondheim, Norway; wenche.sjursen{at}stolav.no
Citation
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers
Publication history
- Received January 29, 2010
- Accepted March 27, 2010
- First published June 28, 2010.
Online issue publication
November 17, 2016
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.