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Showing results (41-50 of 218) with videos related to

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BMC Medical Genetics|March 26, 2017
A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2Bangqing Huang, Yanping Liu, Xue Gao, et al.
Mitochondrion|May 22, 2013
Phenotype and genotype of deaf patients with combined genomic and mitochondrial inheritance modelsShasha Huang, Guojian Wang, Yi Jiang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 14, 2013
[Speech and pitch perception with the new fine structure speech coding strategy]Ping Gu, Xin Xi, Dongyi Han, et al.
Acta Oto-Laryngologica|May 25, 2019
Application of multiplanar reconstruction of spiral CT in the diagnosis and treatment of enlarged vestibular aqueductsBo Gao, Yi Jiang, Shasha Huang, et al.
Journal of Otology|June 26, 2018
A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiencyJing Zou, Xiangqiang Duan, Guiliang Zheng, et al.
BMC Medical Genomics|May 19, 2026
Disparities in deafness gene mutations between Han and Li ethnic newborns in Hainan, China: insights from a combined screening programXin Qi, Dan Wang, Shuo Liu, et al.
Chinese Medical Journal|April 10, 2002
Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
Clinical Characteristics, Surgical Outcomes, and Recurrence Factors of Cerebrospinal Fluid Otorrhea Associated With Inner Ear Malformations: A Retrospective Cohort StudyShao-Hua Wu, Xin Cheng, Shuo Liu, et al.
Chinese Medical Journal|November 2, 2002
Cochlear mitochondrial DNA3867bp deletion in aged miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
International Journal of Pediatric Otorhinolaryngology|November 7, 2017
The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese populationShasha Huang, Bangqing Huang, Guojian Wang, et al.
Pageof 22

Showing results (41-50 of 218) with videos related to

Sort By:
Pageof 22
BMC Medical Genetics|March 26, 2017
A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2Bangqing Huang, Yanping Liu, Xue Gao, et al.
Mitochondrion|May 22, 2013
Phenotype and genotype of deaf patients with combined genomic and mitochondrial inheritance modelsShasha Huang, Guojian Wang, Yi Jiang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 14, 2013
[Speech and pitch perception with the new fine structure speech coding strategy]Ping Gu, Xin Xi, Dongyi Han, et al.
Acta Oto-Laryngologica|May 25, 2019
Application of multiplanar reconstruction of spiral CT in the diagnosis and treatment of enlarged vestibular aqueductsBo Gao, Yi Jiang, Shasha Huang, et al.
Journal of Otology|June 26, 2018
A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiencyJing Zou, Xiangqiang Duan, Guiliang Zheng, et al.
BMC Medical Genomics|May 19, 2026
Disparities in deafness gene mutations between Han and Li ethnic newborns in Hainan, China: insights from a combined screening programXin Qi, Dan Wang, Shuo Liu, et al.
Chinese Medical Journal|April 10, 2002
Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
Clinical Characteristics, Surgical Outcomes, and Recurrence Factors of Cerebrospinal Fluid Otorrhea Associated With Inner Ear Malformations: A Retrospective Cohort StudyShao-Hua Wu, Xin Cheng, Shuo Liu, et al.
Chinese Medical Journal|November 2, 2002
Cochlear mitochondrial DNA3867bp deletion in aged miceXinxin Zhang, Dongyi Han, Dalian Ding, et al.
International Journal of Pediatric Otorhinolaryngology|November 7, 2017
The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese populationShasha Huang, Bangqing Huang, Guojian Wang, et al.
Pageof 22