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Pu Dai

Showing results (11-20 of 238) with videos related to

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Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 3, 2022
[Clinical case analysis and literature review of mandibulofacial dysostosis with microcephaly syndrome]Xiaoyu Li, Mengdi Hong, Pu Dai, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 27, 2014
[Noise-induced hearing loss and cell mechanism of pathophysiology]Qinglei Dai, Xijun Xue, Xukun Yan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 26, 2012
[PCR-GeneScan technique for detection of the GJB2 235 delC and mtDNA A1555G mutations for hereditary hearing loss]Qi Li, Ruping Fang, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 28, 2024
[Baroreflex failure syndrome after the resection of complex paragangliomas of head and neck: a case report]Nan Wu, Guojian Wang, Weidong Shen, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|December 24, 2010
[Diagnostic function of SLC26A4 hot spot mutations screening to enlarged vestibular aqueduct syndrome]Qi Li, Ruping Fang, Yiwen You, et al.
American Journal of Otolaryngology|April 11, 2026
Diagnosis and management of spontaneous CSF otorrhea associated with skull base defectsShaohua Wu, Lang Xu, Shuo Liu, et al.
Journal of Translational Medicine|May 13, 2015
A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafnessAiping Huang, Yongyi Yuan, Yanping Liu, et al.
Plos One|June 11, 2015
The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese IndividualsShasha Huang, Bangqing Huang, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|March 11, 2015
[The study of GJB2 dominant mutaion distribution in Chinese deafness patient and the analysis of phenotype]Shasha Huang, Bangqing Huang, Yongyi Yuan, et al.
Journal of Otology|June 26, 2018
A novel mutation in <i>POU3F4</i> in a Chinese family with X-linked non-syndromic hearing lossBang-Qing Huang, Jia-Ling Zeng, Yong-Yi Yuan, et al.
Pageof 24

Showing results (11-20 of 238) with videos related to

Sort By:
Pageof 24
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 3, 2022
[Clinical case analysis and literature review of mandibulofacial dysostosis with microcephaly syndrome]Xiaoyu Li, Mengdi Hong, Pu Dai, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 27, 2014
[Noise-induced hearing loss and cell mechanism of pathophysiology]Qinglei Dai, Xijun Xue, Xukun Yan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 26, 2012
[PCR-GeneScan technique for detection of the GJB2 235 delC and mtDNA A1555G mutations for hereditary hearing loss]Qi Li, Ruping Fang, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 28, 2024
[Baroreflex failure syndrome after the resection of complex paragangliomas of head and neck: a case report]Nan Wu, Guojian Wang, Weidong Shen, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|December 24, 2010
[Diagnostic function of SLC26A4 hot spot mutations screening to enlarged vestibular aqueduct syndrome]Qi Li, Ruping Fang, Yiwen You, et al.
American Journal of Otolaryngology|April 11, 2026
Diagnosis and management of spontaneous CSF otorrhea associated with skull base defectsShaohua Wu, Lang Xu, Shuo Liu, et al.
Journal of Translational Medicine|May 13, 2015
A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafnessAiping Huang, Yongyi Yuan, Yanping Liu, et al.
Plos One|June 11, 2015
The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese IndividualsShasha Huang, Bangqing Huang, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|March 11, 2015
[The study of GJB2 dominant mutaion distribution in Chinese deafness patient and the analysis of phenotype]Shasha Huang, Bangqing Huang, Yongyi Yuan, et al.
Journal of Otology|June 26, 2018
A novel mutation in <i>POU3F4</i> in a Chinese family with X-linked non-syndromic hearing lossBang-Qing Huang, Jia-Ling Zeng, Yong-Yi Yuan, et al.
Pageof 24