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Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|June 30, 2009
[Audiological and genetic studies on 130 infants with hearing loss]Da-yong Wang, Qiu-ju Wang, Lan Lan, et al.
Acta Oto-Laryngologica|November 20, 2013
Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndromeFei-Fan Zhao, Lan Lan, Da-Yong Wang, et al.
World Journal of Otorhinolaryngology - Head and Neck Surgery|September 5, 2024
Clinical characteristics of sudden hearing loss during pregnancyXiao-Nan Wu, Hong-Yang Wang, Xiao-Long Zhang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 11, 2013
[Clinical analysis of sudden sensorineural hearing loss in patients with different ages]Da-yong Wang, Zhi-qiang Hou, Yan Liu, et al.
Chinese Medical Journal|January 25, 2018
Comparison between Bilateral and Unilateral Sudden Sensorineural Hearing LossDan Bing, Da-Yong Wang, Lan Lan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 29, 2019
Serum Bilirubin Level as a Potential Marker for the Hearing Outcome in Severe-Profound Bilateral Sudden DeafnessDan Bing, Da-Yong Wang, Lan Lan, et al.
Acta Oto-Laryngologica|February 16, 2008
GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjectsYu-Fen Guo, Xiao-Wen Liu, Jing Guan, et al.
Chinese Medical Journal|December 16, 2015
Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing ImpairmentHong-Yang Wang, Ya-Li Zhao, Qiong Liu, et al.
Genetic Testing and Molecular Biomarkers|April 15, 2011
Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 geneFei-Fan Zhao, Yu-Bin Ji, Da-Yong Wang, et al.
Acta Oto-Laryngologica|December 18, 2010
Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in ChinaYu-bin Ji, Dong-Yi Han, Lan Lan, et al.
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