Meng-xia Ni

A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: a case report

X. Xia, Shuai-mei Liu, Ming-chao Zhang, 2017, BMC Pediatrics.

Application of next‑generation sequencing for molecular diagnosis in a large family with osteogenesis imperfecta type I.

X. Xia, Shuai-mei Liu, Meng-xia Ni, 2017, Molecular medicine reports.

Predictive value of GGN and CAG repeat polymorphisms of androgen receptors in testicular cancer: a meta-analysis

X. Xia, Shuai-mei Liu, Ming-chao Zhang, 2016, Oncotarget.

A novel missense mutation of ADAR1\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\textit{ADAR1}$$\end{document} gene

Shuai-mei Liu, Ming-chao Zhang, Meng-xia Ni, 2017, Journal of Genetics.

A novel missense mutation of ADAR1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review.

Shuai-mei Liu, Ming-chao Zhang, Meng-xia Ni, 2017, Journal of genetics.

The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells.

Xiaojun Li, X. Xia, Shuai-mei Liu, 2017, Biochemical and biophysical research communications.