← Evidence map

ArticleOncotarget2017

A novel heterozygous germline deletion in MSH2 gene in a five generation Chinese family with Lynch syndrome.

Bin Wu et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

6 papers cite it

2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 28903413