Beiping Zeng
Zhengzhou, 450052, China
Last Updated: 09/26/2026
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Found 8 publications
Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants.
Journal: Biology
Published: November 18, 2022
Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing.
Journal: Frontiers in genetics
Published: September 29, 2022
A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient.
Journal: BMC medical genomics
Published: July 02, 2022
A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family.
Journal: Chinese medical journal
Published: January 28, 2022
Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome.
Journal: Frontiers in genetics
Published: August 27, 2021
Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.
Journal: Molecular genetics & genomic medicine
Published: January 20, 2021
High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.
Journal: Frontiers in genetics
Published: December 18, 2020
Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.
Journal: Molecular genetics & genomic medicine
Published: May 02, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026