Publications by authors named "Lingfeng Qu"

Claim this Profile
A
A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.
Haiou Jiang, Youya Niu, Lingfeng Qu, Xueshuang Huang, Xinlong Zhu

Biosci Trends· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Congenital cataract in a pedigree with six cases].
Le Wang, Lingfeng Qu, Xinlong Zhu, Mengjin Zhu, Yanrui Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis