Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome-Reference-Cited by-同舟云学术

Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome

Published:2021-04-21 Issue:8 Volume:60 Page:571-576
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Yang Ciyu¹,Li Yirong¹,Trottier Magan²,Farrell Michael P.³,Rai Vikas K.¹,Salo‐Mullen Erin²,Gallagher David J.³,Stadler Zsofia K.²,van der Klift Heleen M.⁴,Zhang Liying¹⁵^ORCID

Affiliation:

1. Department of Pathology Memorial Sloan Kettering Cancer Center New York New York USA

2. Department of Medicine Memorial Sloan Kettering Cancer Center New York New York USA

3. Department of Cancer Genetics Mater Private Hospital Dublin Ireland

4. Department of Clinical Genetics Leiden University Medical Centre Leiden The Netherlands

5. Department of Pathology and Laboratory Medicine David Geffen School of Medicine, University of California Los Angeles California USA

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22950

Reference28 articles.

1. The Incidence of Lynch Syndrome

2. The genetic basis of Lynch syndrome and its implications for clinical practice and risk management

3. Update on Hereditary Colorectal Cancer

4. The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside

5. Inversion of exons 1–7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population

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