Associated Papers
Whole-exome sequencing reveals a comprehensive germline mutation landscape and identifies twelve novel predisposition genes in Chinese prostate cancer patients.
Liang Y et al.
Plos Genetics, 2022
36095024 (PubMed )
Supplement: pgen.1010373.s019.xlsx › S4_Table
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family.
Norouzi M et al.
Frontiers in Oncology, 2021
A Germline CHEK2 Mutation in a Family with Papillary Thyroid Cancer.
Zhao Y et al.
Thyroid : Official Journal of the American Thyroid Association, 2020
A Novel WRN Frameshift Mutation Identified by Multiplex Genetic Testing in a Family with Multiple Cases of Cancer.
Yang L et al.
Plos One, 2015
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