Germline and Tumor Sequencing as a Diagnostic Tool To Resolve Suspected Lynch Syndrome

Author:

Pope Bernard J.ORCID,Clendenning MarkORCID,Rosty Christophe,Mahmood Khalid,Georgeson PeterORCID,Joo Jihoon E.ORCID,Walker Romy,Hutchinson Ryan A.,Jayasekara Harindra,Joseland SharelleORCID,Como Julia,Preston Susan,Spurdle Amanda B.,Macrae Finlay A.,Win Aung K.,Hopper John L.,Jenkins Mark A.,Winship Ingrid M.,Buchanan Daniel D.ORCID

Funder

National Institutes of Health

National Health and Medical Research Council

Publisher

Elsevier BV

Subject

Molecular Medicine,Pathology and Forensic Medicine

Reference82 articles.

1. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1;Ligtenberg;Nat Genet,2009

2. Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study;Win;J Clin Oncol,2012

3. Microsatellite instability in cancer of the proximal colon;Thibodeau;Science,1993

4. Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome);Buchanan;Appl Clin Genet,2014

5. Interobserver variability in the evaluation of mismatch repair protein immunostaining;Klarskov;Hum Pathol,2010

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3