Publications by authors named "Beiping Zeng"

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Molecular Mechanisms and Clinical Phenotypes of Missense Variants.
Lu Mao, Yueqiang Wang, Lei An, Beiping Zeng, Yanyan Wang

Biology (Basel)· March 2023

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Molecular diagnosis of hereditary deafness and application of stepwise testing strategy.
Bei-Ping Zeng, Hon-Gen Xu, Lu Mao, Wen-Xue Tang

Yi Chuan· January 2023

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Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing.
Beiping Zeng, Hongen Xu, Yanan Yu, Siqi Li, Yongan Tian, Zengguang Yang

Front Genet· December 2022

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A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family.
Beiping Zeng, Hongen Xu, Yongan Tian, Qianyu Lin, Haifeng Feng

Chin Med J (Engl)· November 2022

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A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient.
Bin Zuo, Hongen Xu, Zhaoyu Pan, Lu Mao, Haifeng Feng, Beiping Zeng

BMC Med Genomics· October 2022

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Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome.
Haifeng Feng, Hongen Xu, Bei Chen, Shuping Sun, Rongqun Zhai, Beiping Zeng

Front Genet· November 2021

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Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.
Yongan Tian, Hongen Xu, Danhua Liu, Juanli Zhang, Zengguang Yang, Beiping Zeng

Mol Genet Genomic Med· August 2021

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High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.
Sen Zhang, Hongen Xu, Yongan Tian, Danhua Liu, Xinyue Hou, Beiping Zeng

Front Genet· June 2021

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Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.
Yanfang Mi, Danhua Liu, Beiping Zeng, Yongan Tian, Hui Zhang

Mol Genet Genomic Med· January 2021

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