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Showing results (31-40 of 218) with videos related to

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Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|June 30, 2009
[Real-time Taqman probe technique system for detecting the MtDNA 1555 A > G mutation.]Yong-Yi Yuan, De-Liang Huang, Dong-Yi Han, et al.
Journal of Translational Medicine|May 4, 2012
SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueductJiandong Zhao, Yongyi Yuan, Jing Chen, et al.
Bioscience Reports|March 8, 2019
Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing lossLihua Wu, Yunliang Liu, Jianman Wu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 4, 2009
[Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China]Yong-yi Yuan, Pu Dai, Qing-wen Zhu, et al.
BMC Medical Genomics|January 22, 2022
Variant analysis of 92 Chinese Han families with hearing lossXiaohua Jin, Shasha Huang, Lisha An, et al.
Acta Oto-Laryngologica|July 12, 2012
Aberrant internal carotid artery causing objective pulsatile tinnitus and conductive hearing lossYue-Shuai Song, Yong-Yi Yuan, Guo-Jian Wang, et al.
Frontiers in Neuroscience|November 29, 2023
Outcomes of cochlear implantation in 75 patients with auditory neuropathyJie Wu, Jiyue Chen, Zhiwei Ding, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2018
Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland ChinaBangqing Huang, Mingyu Han, Guojian Wang, et al.
American Journal of Otolaryngology|December 25, 2019
Retrospective study of Langerhans cell histiocytosis in ear, nose and neckYan Guo, Fei Ning, Guojian Wang, et al.
Biomed Research International|February 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel <i>GJB2</i> Dominant Mutation in a Chinese FamilyShasha Huang, Xue Gao, Yufeng Wang, et al.
Pageof 22

Showing results (31-40 of 218) with videos related to

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Pageof 22
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|June 30, 2009
[Real-time Taqman probe technique system for detecting the MtDNA 1555 A > G mutation.]Yong-Yi Yuan, De-Liang Huang, Dong-Yi Han, et al.
Journal of Translational Medicine|May 4, 2012
SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueductJiandong Zhao, Yongyi Yuan, Jing Chen, et al.
Bioscience Reports|March 8, 2019
Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing lossLihua Wu, Yunliang Liu, Jianman Wu, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 4, 2009
[Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China]Yong-yi Yuan, Pu Dai, Qing-wen Zhu, et al.
BMC Medical Genomics|January 22, 2022
Variant analysis of 92 Chinese Han families with hearing lossXiaohua Jin, Shasha Huang, Lisha An, et al.
Acta Oto-Laryngologica|July 12, 2012
Aberrant internal carotid artery causing objective pulsatile tinnitus and conductive hearing lossYue-Shuai Song, Yong-Yi Yuan, Guo-Jian Wang, et al.
Frontiers in Neuroscience|November 29, 2023
Outcomes of cochlear implantation in 75 patients with auditory neuropathyJie Wu, Jiyue Chen, Zhiwei Ding, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2018
Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland ChinaBangqing Huang, Mingyu Han, Guojian Wang, et al.
American Journal of Otolaryngology|December 25, 2019
Retrospective study of Langerhans cell histiocytosis in ear, nose and neckYan Guo, Fei Ning, Guojian Wang, et al.
Biomed Research International|February 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel <i>GJB2</i> Dominant Mutation in a Chinese FamilyShasha Huang, Xue Gao, Yufeng Wang, et al.
Pageof 22