Records 1 - 30
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo.
Current medical science 2021 Aug 41 (4): 673-679.
Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu-
| Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China.
The Journal of international medical research 2021 Apr 49 (4): 3000605211000892.
Duan Shihong, Guo Yufen, Chen Xingjian, Li Yo
| Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.
Medicine 2021 Apr 100 (17): e25647.
Hu Hua, Zhou Peng, Wu Jiayan, Lei Wei, Wang Yang, Yang Ying, Liu Hailia
| Targeted next-generation sequencing of deaf patients from Southwestern China.
Molecular genetics & genomic medicine 2021 Mar e1660.
Li Yunlong, Su Jie, Zhang Jingman, Pei Jiahong, Li Dongmei, Zhang Yinhong, Li Jingyu, Chen Menglang, Zhu Baoshe
| [Analysis of results of concurrent hearing and deafness genetic screening and follow up of 33 911 newborns].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 Jan 38 (1): 32-36.
Lei Jie, Han Luhao, Deng Xi, Long Min, Xiao Yanwei, Lin Xiaowen, Zhang Ji
| Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou, China.
Birth defects research 2021 Jan .
Qi Mingming, Lai Huimin, Xu Lili, Zeng Fanhua, Zhang Jing, Xie Kai
| Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China.
Frontiers in genetics 2021 12 637096.
Cai Luhang, Liu Ya, Xu Yaping, Yang Hang, Lv Lihui, Li Yang, Chen Qiongqiong, Lin Xiaojiang, Yang Yihui, Hu Guangwei, Zheng Guofeng, Zhou Jing, Qian Qiyong, Xu Mei-Ai, Fang Jin, Ding Jianjun, Chen Wei, Gao Jio
| [Result of Sanger sequencing for newborn carriers of single heterozygous variants of GJB2 or SLC26A4 gene by genechip analysis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Nov 37 (11): 1213-1216.
He Jun, Na Yang, Liu Jiya
| Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
Molecular genetics & genomic medicine 2020 Oct e1539.
Xiang Yan-Bao, Xu Chen-Yang, Xu Yun-Zhi, Li Huan-Zheng, Zhou Li-Li, Xu Xue-Qin, Chen Zi-Hui, Tang Shao-H
| Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2020 May .
Chandru Jayasankaran, Jeffrey Justin Margret, Pavithra Amritkumar, Vanniya S Paridhy, Devi G Nandhini, Mahalingam Subathra, Karthikeyen Natarajan Padmavathy, Srisailapathy C R Srikuma
| The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
International journal of pediatric otorhinolaryngology 2020 May 136 110143.
Liu Xiao-Wen, Wang Jian-Chao, Wang Su-Yang, Li Shu-Juan, Zhu Yi-Ming, Ding Wen-Juan, Xu Chen-Yang, Duan Lei, Xu Bai-Cheng, Guo Yu-F
| [Sequencing of 100 common variation sites of 18 deafness susceptibility genes among 16 182 individuals from Dongguan].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Apr 37 (4): 373-377.
Zhang Bashan, Li Chan, Zhu Zhinian, Ding Aijiao, Liu Yuanru, Lei W
| Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Orphanet journal of rare diseases 2020 Jan 15 (1): 29.
Yu Xiaoyu, Lin Yun, Xu Jun, Che Tuanjie, Li Lin, Yang Tao, Wu H
| Mutation analysis of the SLC26A4 gene in three Chinese families.
Bioscience trends 2019 Oct .
Wen Cheng, Wang Shijie, Zhao Xuelei, Wang Xianlei, Wang Xueyao, Cheng Xiaohua, Huang Lih
| Suspension array-based deafness genetic screening in 53,033 Chinese newborns identifies high prevalence of 109?G>A in GJB2.
International journal of pediatric otorhinolaryngology 2019 Aug 126 109630.
Zou Yu, Dai Qi-Qiang, Tao Wei-Jing, Wen Xiao-Ling, Feng De-Feng, Deng Hua, Zhou Wei-Ping, Li Mi, Zhang Lia
| Variations in the Mutational Spectrum in Nonsyndromic Hearing Impairment: A study of the Special Schools for the Deaf in Southern China.
The journal of international advanced otology 2019 Jul .
Lin Ying, Yu Feng, Jiao Yuelong, Zhou Fe
| Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.
Acta oto-laryngologica 2019 May 1-6.
Zhang Meng, Han Yuechen, Zhang Fengguo, Bai Xiaohui, Wang Hai
| Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
International journal of pediatric otorhinolaryngology 2019 Apr 122 185-190.
Xiang Yan-Bao, Tang Shao-Hua, Li Huan-Zheng, Xu Chen-Yang, Chen Chong, Xu Yun-Zhi, Ding Li-Rong, Xu Xue-Q
| Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population.
Scientific reports 2019 Feb 9 (1): 1604.
Han Jae Joon, Nguyen Pham Dinh, Oh Doo-Yi, Han Jin Hee, Kim Ah-Reum, Kim Min Young, Park Hye-Rim, Tran Lam Huyen, Dung Nguyen Huu, Koo Ja-Won, Lee Jun Ho, Oh Seung Ha, Anh Vu Hoang, Choi Byung Yo
| A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China.
Genetic testing and molecular biomarkers 2019 Jan 23 (1): 51-56.
Ming Liang, Wang Yangxia, Lu Wei, Sun Ti
| Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Molecular genetics & genomic medicine 2019 Jan e537.
Zhou Yongan, Li Chao, Li Min, Zhao Zhonghua, Tian Shuxiong, Xia Hou, Liu Peixian, Han Yaxin, Ren Ruirui, Chen Jianping, Jia Caihong, Guo W
| A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss.
PloS one 2019 14 (4): e0215212.
Liu Yalan, Hu Chang, Liu Chang, Liu Deyuan, Mei Lingyun, He Chufeng, Jiang Lu, Wu Hong, Chen Hongsheng, Feng Yo
| [Analysis of mutations of 4 common genes among 216 patients with non-syndromic hearing impairment].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 Oct 35 (5): 630-633.
Li Can, Lu Dan, Chen Xiaoping, Huang Bingcang, Chen Kai, Liu Xing, Hu An, Zhang Yi, Xue Xiaocheng, Xing Yanli, Yan Zhigang, Dong Xiangro
| Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing.
Medicine 2018 Sep 97 (38): e12285.
Zhao Pingsen, Lin Lifang, Lan Liubi
| [Analysis of genotypes and audiological characteristics of children with SLC26A4 gene pathogenic mutations].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2018 Jun 32 (11): 836-840.
Zhao X L, Huang L H, Wang X Y, DU Yt, Wang Xl, Cheng X H, Zhao L P, Li
| Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
International journal of pediatric otorhinolaryngology 2018 May 108 49-54.
Huang Bangqing, Han Mingyu, Wang Guojian, Huang ShaSha, Zeng Jialing, Yuan Yongyi, Dai
| Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.
The Journal of pediatrics 2018 Apr .
Lu Chun-Yi, Tsao Po-Nien, Ke Ying-Ying, Lin Yi-Hsin, Lin Yin-Hung, Hung Chia-Cheng, Su Yi-Ning, Hsu Wei-Chung, Hsieh Wu-Shiun, Huang Li-Min, Wu Chen-Chi, Hsu Chuan-J
| Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.
PloS one 2018 13 (4): e0195740.
Hao Zongjie, Fu Denggang, Ming Yang, Yang Jinlong, Huang Qi, Lin Weilong, Zhang Huan, Zhang Bin, Zhou Aifen, Hu Xijiang, Yao Cong, Dong Yunping, Ring Huijun Z, Ring Brian
| Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.
PloS one 2018 13 (12): e0209797.
Erdenechuluun Jargalkhuu, Lin Yin-Hung, Ganbat Khongorzul, Bataakhuu Delgermaa, Makhbal Zaya, Tsai Cheng-Yu, Lin Yi-Hsin, Chan Yen-Hui, Hsu Chuan-Jen, Hsu Wei-Chung, Chen Pei-Lung, Wu Chen-C
| [An analysis of the mutation in GJB2,GJB3,SLC26A4 and mtDNA12SrRNA in new born].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2017 May 31 (9): 664-666.
Chai F, Zhao H L, Qiu S