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Journal of Human Genetics|September 5, 2022
DNA2 mutation causing multisystemic disorder with impaired mitochondrial DNA maintenanceJiayu Sun, Wenwen Su, Jianwen Deng, et al.Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|September 26, 2021
VASN promotes proliferation of laryngeal cancer cells via YAP/TAZHaotian Liu, Weili Kong, Shuxin Wen, et al.Journal of Clinical Laboratory Analysis|April 28, 2023
Delayed progressive sensorineural hearing loss due to a novel compound heterozygous PTPRQ mutation in a Chinese patientYao Qin, Yi'nan Ma, Zhen'gang Zeng, et al.The Journal of International Advanced Otology|August 14, 2020
Predictors of Conservative Treatment Outcomes for Adult Otitis Media with EffusionZhen Zhong, Junbo Zhang, Lei Ren, et al.Journal of Speech, Language, and Hearing Research : JSLHR|August 29, 2020
Sequential Bilateral Cochlear Implantation With Prolonged Time IntervalsZhikai Zhang, Chaogang Wei, Yanmei Zhang, et al.Chinese Medical Journal|June 17, 2014
Audiological evaluation in Chinese patients with mitochondrial encephalomyopathiesYuhe Liu, Junfang Xue, Danhua Zhao, et al.Journal of Clinical Medicine|January 28, 2026
Association of Hyperbilirubinemia with Lipid Profile and Lipid-Related Diseases: A Large Community-Based Cohort StudyBorong Yu, Yuhe Liu, Wenqian Wu, et al.Hearing Research|March 14, 2026
The neural processing mode and development of emotional prosody in children with cochlear implantsJunsheng Hong, Tianyu Xin, Yuyang Wang, et al.Plos One|July 22, 2015
Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese FamilyJuanjuan Gao, Qi Wang, Cheng Dong, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|October 1, 2013
[Management and classification of first branchial cleft anomalies]Zhen Zhong, Enmin Zhao, Yuhe Liu, et al.Pageof 119