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Dongyang Kang

Showing results (21-30 of 54) with videos related to

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Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
International Journal of Pediatric Otorhinolaryngology|February 8, 2014
Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese familyAiping Huang, Yongyi Yuan, Naichao Duan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2024
Clinical Application of the 4K-3D Exoscope System in Cochlear ImplantationHonglei Zhang, Guojian Wang, Xin Zhang, et al.
Stem Cell Research|June 12, 2022
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10Xiaohong Li, Xue Gao, Shasha Huang, et al.
Human Genetics|June 18, 2021
Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndromeGuojian Wang, Xiaohong Li, Xue Gao, et al.
Analytical Chemistry|July 11, 2018
Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCRFang Wang, Lingxiang Zhu, Baoxia Liu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing lossJianzhong Li, Jing Cheng, Yanping Lu, et al.
Journal of Translational Medicine|December 2, 2008
Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysisPu Dai, Yongyi Yuan, Deliang Huang, et al.
Journal of Translational Medicine|September 12, 2009
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in ChinaYongyi Yuan, Yiwen You, Deliang Huang, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
International Journal of Pediatric Otorhinolaryngology|February 8, 2014
Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese familyAiping Huang, Yongyi Yuan, Naichao Duan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2024
Clinical Application of the 4K-3D Exoscope System in Cochlear ImplantationHonglei Zhang, Guojian Wang, Xin Zhang, et al.
Stem Cell Research|June 12, 2022
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10Xiaohong Li, Xue Gao, Shasha Huang, et al.
Human Genetics|June 18, 2021
Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndromeGuojian Wang, Xiaohong Li, Xue Gao, et al.
Analytical Chemistry|July 11, 2018
Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCRFang Wang, Lingxiang Zhu, Baoxia Liu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 4, 2011
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing lossJianzhong Li, Jing Cheng, Yanping Lu, et al.
Journal of Translational Medicine|December 2, 2008
Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysisPu Dai, Yongyi Yuan, Deliang Huang, et al.
Journal of Translational Medicine|September 12, 2009
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in ChinaYongyi Yuan, Yiwen You, Deliang Huang, et al.
Pageof 6