Clinical exome sequencing identified POLB c.C1002A as a possible genetic cause in a family with hereditary cancer-predisposing syndrome-Reference-Cited by-同舟云学术

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Clinical exome sequencing identified POLB c.C1002A as a possible genetic cause in a family with hereditary cancer-predisposing syndrome

Published:2020-07 Issue: Volume:245 Page:49-52
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Zhu Zhenxin,Wang Jieshi,Jiang Lisha,Lin Ling,Meng Peng,Zhao Jiangman,Cai Qingping

Funder

National Natural Science Foundation of China

Shanghai Natural Science Foundation

Shanghai Shenkang Hospital Development Center

Second Military Medical University

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference18 articles.

1. Environmental and heritable factors in the causation of cancer–analyses of cohorts of twins from Sweden, Denmark, and Finland;Lichtenstein;New England J Med,2000

2. Perspective on oncogenic processes at the end of the beginning of cancer genomics;Ding;Cell,2018

3. Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families;Castera;Genet Med Off J Am College Med Genet,2018

4. Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment;Desmond;JAMA Oncol,2015

5. Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on colorectal cancer;Giardiello;Gastroenterology,2014

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