Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families-Reference-Cited by-同舟云学术

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families

Published:2014-02-20 Issue:1 Volume:135 Page:69-77
ISSN:0020-7136
Container-title:International Journal of Cancer
language:en
Short-container-title:Int. J. Cancer

Author:

Steinke Verena¹,Holzapfel Stefanie¹,Loeffler Markus²,Holinski-Feder Elke³⁴,Morak Monika³⁴,Schackert Hans K.⁵,Görgens Heike⁵,Pox Christian⁶,Royer-Pokora Brigitte⁷,von Knebel-Doeberitz Magnus⁸⁹,Büttner Reinhard¹⁰,Propping Peter¹,Engel Christoph²,

Affiliation:

1. Institute of Human Genetics, University of Bonn; Bonn, Germany

2. Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig; Leipzig, Saxony, Germany

3. Department of Medicine; Ludwig-Maximilians-University; Munich Germany

4. Center of Medical Genetics; Munich Germany

5. Department of Surgical Research; Technische Universität Dresden; Bochum, North Rhine-Westphalia, Germany

6. Department of Medicine; Knappschaftskrankenhaus, Ruhr-University Bochum; Germany

7. Institute of Human Genetics; Medical School; Heinrich Heine University; Duesseldorf Germany

8. Department of Applied Tumor Biology; Institute of Pathology; University Hospital Heidelberg; Heidelberg, Germany

9. Cooperation Unit Applied Tumor Biology; German Cancer Research Center (DKFZ); Heidelberg Germany

10. Institute of Pathology, University of Cologne; Cologne, NRW, Germany

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference18 articles.

1. The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome;Watson;Int J Cancer,2008

2. 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

3. Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany;Lamberti;Digestion,2006

4. Report from the Jerusalem workshop on Lynch syndrome-hereditary nonpolyposis colorectal cancer;Boland;Gastroenterology,2010

5. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications;Lynch;Clin Genet,2009

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