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Biochemical and Biophysical Research Communications
|
August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families
Pu Dai, Yongyi Yuan, Deliang Huang, et al.
Human Genetics
|
June 18, 2021
Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome
Guojian Wang, Xiaohong Li, Xue Gao, et al.
Acta Oto-Laryngologica
|
May 21, 2019
Genotype-phenotype variability in Chinese cases of Treacher Collins syndrome
Xiaohong Li, Yu Su, Shasha Huang, 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 loss
Jianzhong 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 analysis
Pu 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 impairment
Zhengyue Li, Yilian Guo, Yu Lu, et al.
Plos One
|
November 28, 2012
Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China
Yongyi Yuan, Weiwei Guo, Jie Tang, et al.
Journal of Translational Medicine
|
December 18, 2013
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China
Feng Xin, Yongyi Yuan, Xiaoming Deng, et al.
Journal of Translational Medicine
|
September 12, 2009
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China
Yongyi Yuan, Yiwen You, Deliang Huang, et al.
Page
of 22
Search research articles
Search
Showing results (111-120 of 218) with videos related to
Sort By:
Page
of 22
Biochemical and Biophysical Research Communications
|
August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families
Pu Dai, Yongyi Yuan, Deliang Huang, et al.
Human Genetics
|
June 18, 2021
Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome
Guojian Wang, Xiaohong Li, Xue Gao, et al.
Acta Oto-Laryngologica
|
May 21, 2019
Genotype-phenotype variability in Chinese cases of Treacher Collins syndrome
Xiaohong Li, Yu Su, Shasha Huang, 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 loss
Jianzhong 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 analysis
Pu 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 impairment
Zhengyue Li, Yilian Guo, Yu Lu, et al.
Plos One
|
November 28, 2012
Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China
Yongyi Yuan, Weiwei Guo, Jie Tang, et al.
Journal of Translational Medicine
|
December 18, 2013
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China
Feng Xin, Yongyi Yuan, Xiaoming Deng, et al.
Journal of Translational Medicine
|
September 12, 2009
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China
Yongyi Yuan, Yiwen You, Deliang Huang, et al.
Page
of 22