Yongan Tian
3PUBLICATIONS
14CO-AUTHORS
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Publications (3)
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|Apr 14, 2025
Exonic Deletions and Deep Intronic Variants of the SLC26A4 Gene Contribute to the Genetic Diagnosis of Unsolved Patients With Enlarged Vestibular Aqueduct.Yongan Tian, Mengli Liu, Yu Lu
|Jul 14, 2021
Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.Jinying Li, Hongen Xu, Jianfeng Sun
|Jun 25, 2021
Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.Yongan Tian, Hongen Xu, Danhua Liu
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Frequent Collaborators
3 joint publications
Hongen Xu
2 joint publications
Danhua Liu
2 joint publications
Wenxue Tang
1 joint publications
Bei Chen
1 joint publications
Jinying Li
1 joint publications
Jianfeng Sun
1 joint publications
Yaping Qin
1 joint publications
Ruijun Li
1 joint publications
Lingling Neng
1 joint publications
Xiaohua Deng
