H. Yuan

A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China

L. Lan, J. Guan, Bai-cheng Xu, 2007, Clinical genetics.

Target-Sequencing of Female Infertility Pathogenic Gene Panel and a Novel TUBB8 Loss-of-Function Mutation

N. Li, Ruizhi Feng, Yanni He, 2022, Frontiers in Genetics.

Audiological and genetic features of the mtDNA mutations

X. Liu, D. Yan, S. Angeli, 2008, Acta oto-laryngologica.

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

S. Z. Yang, D. Yan, G. Feng, 2008, Clinical genetics.

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

S. Schwartz, C. Lee, C. Morton, 2001, Human molecular genetics.

AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23–27.3

Q. Z. Li, S. Leal, J. Guan, 2005, Journal of Medical Genetics.

[Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].

S. Jiang, W. Yang, P. Dai, 1999, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.