Huanfei Liu

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

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

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease

D. Frishman, Hongen Xu, Jiancheng Guo, 2021, npj Genomic Medicine.

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease

D. Frishman, Hongen Xu, Jiancheng Guo, 2021, NPJ genomic medicine.

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients

W. Lu, Hongen Xu, Wenxue Tang, 2020, Molecular genetics & genomic medicine.

Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families

W. Lu, Hongen Xu, Wenxue Tang, 2020, BioMed research international.

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

Hongen Xu, Wenxue Tang, Chang Yu, 2021, BioMed research international.

Perrault syndrome: Clinical report and retrospective analysis

W. Lu, Hongen Xu, Wenxue Tang, 2020, Molecular genetics & genomic medicine.

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.