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Pu Dai

Showing results (91-100 of 218) with videos related to

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Journal of Translational Medicine|November 16, 2012
Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counselingQi Li, Qing-wen Zhu, Yong-yi Yuan, et al.
Heliyon|March 19, 2024
Mitochondrial tRNA<sup>Ser(UCN)</sup> mutations associated non-syndromic sensorineural hearing loss in Chinese familiesDejun Zhang, Jie Wu, Yongyi Yuan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2010
[GJB2 235delC single allelic mutation modulates the phenotype associated with the mitochondrial A1555G mutation]Qi Li, Ru-ping Fang, Hong-gen Zhou, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 17, 2012
[Prenatal genetic counseling and instruction for deaf families by genetic test]Ming-yu Han, Sha-sha Huang, Guo-jian Wang, et al.
International Journal of Pediatric Otorhinolaryngology|May 12, 2015
Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reactionShasha Huang, Guangxin Xiang, Dongyang Kang, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 26, 2014
Congenital middle ear abnormalities with absence of the oval window: diagnosis, surgery, and audiometric outcomesYu Su, Hu Yuan, Yue-shuai Song, et al.
BMC Genetics|February 19, 2014
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutationYuhua Zhu, Shasha Huang, Dongyang Kang, et al.
Biosensors & Bioelectronics|June 17, 2011
Validation of a mobile phone-assisted microarray decoding platform for signal-enhanced mutation detectionGuanbin Zhang, Caixia Li, Yuan Lu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|July 17, 2007
[Reconstruction and analysis of three-dimensional finite element model of human middle ear]Guan-Ping Zhang, Ai-Xia Wu, Pu Dai, et al.
Plos One|August 8, 2015
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaYi Jiang, Shasha Huang, Tao Deng, et al.
Pageof 22

Showing results (91-100 of 218) with videos related to

Sort By:
Pageof 22
Journal of Translational Medicine|November 16, 2012
Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counselingQi Li, Qing-wen Zhu, Yong-yi Yuan, et al.
Heliyon|March 19, 2024
Mitochondrial tRNA<sup>Ser(UCN)</sup> mutations associated non-syndromic sensorineural hearing loss in Chinese familiesDejun Zhang, Jie Wu, Yongyi Yuan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2010
[GJB2 235delC single allelic mutation modulates the phenotype associated with the mitochondrial A1555G mutation]Qi Li, Ru-ping Fang, Hong-gen Zhou, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 17, 2012
[Prenatal genetic counseling and instruction for deaf families by genetic test]Ming-yu Han, Sha-sha Huang, Guo-jian Wang, et al.
International Journal of Pediatric Otorhinolaryngology|May 12, 2015
Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reactionShasha Huang, Guangxin Xiang, Dongyang Kang, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 26, 2014
Congenital middle ear abnormalities with absence of the oval window: diagnosis, surgery, and audiometric outcomesYu Su, Hu Yuan, Yue-shuai Song, et al.
BMC Genetics|February 19, 2014
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutationYuhua Zhu, Shasha Huang, Dongyang Kang, et al.
Biosensors & Bioelectronics|June 17, 2011
Validation of a mobile phone-assisted microarray decoding platform for signal-enhanced mutation detectionGuanbin Zhang, Caixia Li, Yuan Lu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|July 17, 2007
[Reconstruction and analysis of three-dimensional finite element model of human middle ear]Guan-Ping Zhang, Ai-Xia Wu, Pu Dai, et al.
Plos One|August 8, 2015
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaYi Jiang, Shasha Huang, Tao Deng, et al.
Pageof 22