Search research articles
Contact Us
Filters
Showing results (161-170 of 218) with videos related to
Page
of 22
Sort By:
European Journal of Human Genetics : EJHG
|
September 22, 2019
Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls
Yongyi Yuan, Qi Li, Yu Su, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
September 4, 2018
Skewed X-chromosome inactivation and next-generation sequencing to identify a novel SMPX variants associated with X-linked hearing loss in a Chinese family
Song Gao, Yi Jiang, Guojian Wang, et al.
Human Mutation
|
October 22, 2014
Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99
Jiangxia Li, Xiaohan Zhao, Qian Xin, et al.
Human Mutation
|
December 29, 2007
Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening
Cai-Xia Li, Qian Pan, Yong-Gang Guo, et al.
Acta Oto-Laryngologica
|
June 7, 2012
Intraoperative CT-guided cochlear implantation in congenital ear deformity
Yong-Yi Yuan, Yue-Shuai Song, Ci-Man Chai, et al.
Frontiers in Genetics
|
June 17, 2022
Genetic Analysis of the <i>LOXHD1</i> Gene in Chinese Patients With Non-Syndromic Hearing Loss
Wei-Qian Wang, Xue Gao, Sha-Sha Huang, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2015
Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss
Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
January 18, 2006
[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients]
Pu Dai, Fei Yu, Dong-yang Kang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
December 7, 2007
[Prenatal diagnosis for hereditary deaf families assisted by genetic testing]
Bing Han, Pu Dai, Qing-wei Qi, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 218) with videos related to
Sort By:
Page
of 22
European Journal of Human Genetics : EJHG
|
September 22, 2019
Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls
Yongyi Yuan, Qi Li, Yu Su, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
September 4, 2018
Skewed X-chromosome inactivation and next-generation sequencing to identify a novel SMPX variants associated with X-linked hearing loss in a Chinese family
Song Gao, Yi Jiang, Guojian Wang, et al.
Human Mutation
|
October 22, 2014
Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99
Jiangxia Li, Xiaohan Zhao, Qian Xin, et al.
Human Mutation
|
December 29, 2007
Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening
Cai-Xia Li, Qian Pan, Yong-Gang Guo, et al.
Acta Oto-Laryngologica
|
June 7, 2012
Intraoperative CT-guided cochlear implantation in congenital ear deformity
Yong-Yi Yuan, Yue-Shuai Song, Ci-Man Chai, et al.
Frontiers in Genetics
|
June 17, 2022
Genetic Analysis of the <i>LOXHD1</i> Gene in Chinese Patients With Non-Syndromic Hearing Loss
Wei-Qian Wang, Xue Gao, Sha-Sha Huang, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2015
Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss
Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
January 18, 2006
[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients]
Pu Dai, Fei Yu, Dong-yang Kang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
December 7, 2007
[Prenatal diagnosis for hereditary deaf families assisted by genetic testing]
Bing Han, Pu Dai, Qing-wei Qi, et al.
Page
of 22