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Pu Dai

Showing results (151-160 of 218) with videos related to

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Research (Washington, D.C.)|January 19, 2026
The Optically Guided and Pre-assembled Implantation Cranial Window Reveals Cortical Spatial Representations during NavigationWeihao Zhao, Lin Gao, Yu Wu, et al.
Chinese Medical Journal|June 5, 2009
Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairmentBing Han, Jing Cheng, Shu-Zhi Yang, et al.
Yi Chuan = Hereditas|April 22, 2008
[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2]Jing Chen, Shu-Zhi Yang, Jun Liu, et al.
Gene Expression Patterns : GEP|December 30, 2021
Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunctionWei-Qian Wang, Shi-Wei Qiu, Sha-Sha Huang, et al.
Head & Face Medicine|July 25, 2023
Surgical management and the prognosis of iatrogenic facial nerve injury in middle ear surgery: a 20-year experienceJianbin Sun, Ruoya Wang, Xingrui Chen, et al.
European Journal of Radiology|July 14, 2026
Deep learning for subtype classification of inner ear malformations on temporal bone HRCT: Development and multicenter validationXiaoge Li, Xing Zhao, Qianyu Hao, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|May 23, 2006
[Genotypic analysis of familial dilated vestibular aqueduct syndrome]Pu Dai, Dongyi Han, Juyang Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 5, 2020
[Clinical practice guidelines for hereditary non-syndromic deafness]Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Huijun Yuan, Pu Dai, et al.
Journal of Medical Genetics|August 2, 2020
Congenital sensorineural hearing loss as the initial presentation of <i>PTPN11</i>-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanismsXue Gao, Sha-Sha Huang, Shi-Wei Qiu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|March 30, 2012
[Prenatal genetic test and clinical guidance for 213 hereditary deaf families]Ming-yu Han, Yan-ping Lu, Xu-ming Bian, et al.
Pageof 22

Showing results (151-160 of 218) with videos related to

Sort By:
Pageof 22
Research (Washington, D.C.)|January 19, 2026
The Optically Guided and Pre-assembled Implantation Cranial Window Reveals Cortical Spatial Representations during NavigationWeihao Zhao, Lin Gao, Yu Wu, et al.
Chinese Medical Journal|June 5, 2009
Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairmentBing Han, Jing Cheng, Shu-Zhi Yang, et al.
Yi Chuan = Hereditas|April 22, 2008
[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2]Jing Chen, Shu-Zhi Yang, Jun Liu, et al.
Gene Expression Patterns : GEP|December 30, 2021
Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunctionWei-Qian Wang, Shi-Wei Qiu, Sha-Sha Huang, et al.
Head & Face Medicine|July 25, 2023
Surgical management and the prognosis of iatrogenic facial nerve injury in middle ear surgery: a 20-year experienceJianbin Sun, Ruoya Wang, Xingrui Chen, et al.
European Journal of Radiology|July 14, 2026
Deep learning for subtype classification of inner ear malformations on temporal bone HRCT: Development and multicenter validationXiaoge Li, Xing Zhao, Qianyu Hao, et al.
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|May 23, 2006
[Genotypic analysis of familial dilated vestibular aqueduct syndrome]Pu Dai, Dongyi Han, Juyang Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 5, 2020
[Clinical practice guidelines for hereditary non-syndromic deafness]Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Huijun Yuan, Pu Dai, et al.
Journal of Medical Genetics|August 2, 2020
Congenital sensorineural hearing loss as the initial presentation of <i>PTPN11</i>-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanismsXue Gao, Sha-Sha Huang, Shi-Wei Qiu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|March 30, 2012
[Prenatal genetic test and clinical guidance for 213 hereditary deaf families]Ming-yu Han, Yan-ping Lu, Xu-ming Bian, et al.
Pageof 22