Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes-Reference-Cited by-同舟云学术

Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes

Published:2019-07-18 Issue:5 Volume:22 Page:681-693
ISSN:1699-048X
Container-title:Clinical and Translational Oncology
language:en
Short-container-title:Clin Transl Oncol

Author:

Golyan F. F.,Druley T. E.,Abbaszadegan M. R.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12094-019-02174-z.pdf

Reference33 articles.

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2. Wen X-D, et al. Earlier onset and multiple primaries in familial as opposed to sporadic esophageal cancer. World. 2014;2:005.

3. Stoner GD, Gupta A. Etiology and chemoprevention of esophageal squamous cell carcinoma. Carcinogenesis. 2001;22(11):1737–46.

4. Mir MM, et al. p53 mutation profile of squamous cell carcinomas of the esophagus in Kashmir (India): a high-incidence area. Int J Cancer. 2005;116(1):62–8.

5. Su H, et al. Gene expression analysis of esophageal squamous cell carcinoma reveals consistent molecular profiles related to a family history of upper gastrointestinal cancer. Can Res. 2003;63(14):3872–6.

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