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Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2).
Eur J Hum Genet. 2010 Sep;18(9). doi: 10.1038/ejhg.2009.232. Epub 2010 Jan 27.
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Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012.
Eur J Hum Genet. 2013 Jan;21(1). doi: 10.1038/ejhg.2012.164. Epub 2012 Aug 15.
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Evaluation and management of Lynch syndrome.
Clin Adv Hematol Oncol. 2007 Nov;5(11):851,873.
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Mismatch repair gene deficiency and genetic anticipation in Lynch syndrome: myth or reality?
Dis Colon Rectum. 2015 Jan;58(1):141-2. doi: 10.1097/DCR.0000000000000275.

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Unique Combination of Diamond-Blackfan Anemia and Lynch Syndrome in Adult Female: A Case Report.
Front Oncol. 2021 Apr 16;11:652696. doi: 10.3389/fonc.2021.652696. eCollection 2021.
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Patient compliance based on genetic medicine: a literature review.
J Community Genet. 2014 Jan;5(1):31-48. doi: 10.1007/s12687-013-0160-2. Epub 2013 Aug 10.
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The challenge of implementing genetic tests with clinical utility while avoiding unsound applications.
J Community Genet. 2014 Jan;5(1):7-12. doi: 10.1007/s12687-012-0121-1. Epub 2012 Oct 9.
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Clinical utility gene card for: familial adenomatous polyposis (FAP) and attenuated FAP (AFAP).
Eur J Hum Genet. 2011 Jul;19(7). doi: 10.1038/ejhg.2011.7. Epub 2011 Feb 2.

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