Beiping Zeng

Early truncation of the N‐terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype

Hongen Xu, Wenxue Tang, Yulin Zhao, 2020, Molecular genetics & genomic medicine.

Juvenile-onset motor neuron disease caused by novel mutations in β-hexosaminidase.

R. Finkel, T. Pierson, G. Tennekoon, 2013, Molecular genetics and metabolism.

A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient

Hongen Xu, Wenxue Tang, Beiping Zeng, 2022, BMC Medical Genomics.

Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing

Hongen Xu, Wenxue Tang, Yanan Yu, 2022, Frontiers in Genetics.

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Frontiers in Genetics.

Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome

Shuping Sun, Hongen Xu, Wenxue Tang, 2021, Frontiers in Genetics.

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Molecular genetics & genomic medicine.

Juvenile-onset G(M2)-gangliosidosis in an African-American child with nystagmus.

S. Rosengren, A. Paciorkowski, E. Kolodny, 2008, Pediatric neurology.