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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.Biochemical and Biophysical Research Communications|August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese familiesPu Dai, Yongyi Yuan, Deliang Huang, et al.Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|July 15, 2006
[Surgical approach and materials in reparation of cerebrospinal rhinorrhea (54 cases reports)]Yungao Zhang, Rongguang Wang, Wenming Wu, 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.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 31, 2010
[Research on mitochondrial DNA T1095C gene variation in military noise-induced hearing loss]Li Qu, Xijun Xue, Pu Dai, et al.Plos One|August 13, 2013
Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairmentZhengyue Li, Yilian Guo, Yu Lu, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|April 30, 2024
[Clinical characteristics and prognosis of two anastomosis techniques in the treatment of facial nerve defects]Shuhang Fan, Jianbin Sun, Qin Wang, et al.Plos One|March 6, 2012
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairmentYongyi Yuan, Xun Zhang, Shasha Huang, et al.American Journal of Medical Genetics. Part A|September 7, 2006
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing lossWie-Yen Young, Lidong Zhao, Yaping Qian, et al.Pageof 30