Shaohua Tang
6PUBLICATIONS
3CO-AUTHORS
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Publications (6)
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|Feb 24, 2025
Saliva Sample-Based Non-Invasive Carrier Screening for Spinal Muscular Atrophy, Hereditary Hearing Loss, and Thalassemia in 13,926 Women of Reproductive Age From South Zhejiang.Chenyang Xu, Yanbao Xiang, Xiaoling Lin
|Sep 27, 2022
Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss.Yanbao Xiang, Chenyang Xu, Yunzhi Xu
|Nov 12, 2021
The distal arthrogryposis-linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3.Jinfang Lu, Huanzheng Li, He Zhang
|May 21, 2021
The variations in human orphan G protein-coupled receptor QRFPR affect PI3K-AKT-mTOR signaling.Huanzheng Li, Ran Lou, Xueqin Xu
|Oct 30, 2020
Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism.Chenyang Xu, Yanbao Xiang, Huanzheng Li
|Oct 23, 2020
Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.Yan-Bao Xiang, Chen-Yang Xu, Yun-Zhi Xu
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