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 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
| [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
| 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
| 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
| 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
| 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 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
| 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
| 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
| GJB3/GJB6 screening in GJB2 carriers with idiopathic hearing loss: Is it necessary?
Journal of clinical laboratory analysis 2018 Jun e22592.
Chen Kaitian, Wu Xuan, Zong Ling, Jiang Hongy
| Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations.
Iranian journal of public health 2018 Jan 47 (1): 95-102.
Naseri Marzieh, Akbarzadehlaleh Masoud, Masoudi Marjan, Ahangari Najmeh, Poursadegh Zonouzi Ali Akbar, Poursadegh Zonouzi Ahmad, Shams Leila, Nejatizadeh Az
| [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
| Hearing-loss-associated gene detection in neonatal intensive care unit.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2017 Jan 1-12.
Yang S M, Liu Ying, Liu C, Yin A H, Wu Y F, Zheng X E, Yang H M, Yang
| A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.
PloS one 2017 12 (5): e0177196.
Li Siping, Peng Qi, Liao Shengyun, Li Wenrui, Ma Qiang, Lu Xiaom
| Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region.
Genetics and molecular biology 2016 Oct 0.
Liu Yongzhi, Ao Liying, Ding Haitao, Zhang Dong
| Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.
Genetic testing and molecular biomarkers 2016 Sep .
Chen Siqi, Dong Cheng, Wang Qi, Zhong Zhen, Qi Yu, Ke Xiaomei, Liu Yu
| Analysis of p.V37I compound heterozygous mutations in the GJB2 gene in Chinese infants and young children.
Bioscience trends 2016 Jun .
Du Yating, Huang Lihui, Cheng Xiaohua, Zhao Liping, Ruan Yu, Ni Tingti
| Genotypes and phenotypes of a family with a deaf child carrying combined heterozygous mutations in SLC26A4 and GJB3 genes.
Molecular medicine reports 2016 May .
Li Yunlong, Zhu Baoshe
| Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?
Medicine 2016 Apr 95 (14): e3029.
Kim So Young, Kim Ah Reum, Kim Nayoung K D, Lee Chung, Kim Min Young, Jeon Eun-Hee, Park Woong-Yang, Choi Byung Yo
| Deafness gene mutations in newborns in Beijing.
Acta oto-laryngologica 2016 Jan 1-5.
Han Shujing, Yang Xiaojian, Zhou Yi, Hao Jinsheng, Shen Adong, Xu Fang, Chu Ping, Jin Yaqiong, Lu Jie, Guo Yongli, Shi Jin, Liu Haihong, Ni X
| Screening and analysis of mutation hot-spots in deafness-associated genes among adolescents with hearing loss.
Molecular medicine reports 2015 Oct .
Jiang Hong, Liu Qizhen, Chen Liho
| Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China.
Clinical and experimental otorhinolaryngology 2015 Sep 8 (3): 211-7.
Li Shou-Xia, Chen Ding-Li, Zhao Su-Bin, Guo Li-Li, Feng Hai-Qin, Zhang Xiao-Fang, Ping Li-Li, Yang Zhi-Ming, Sun Cai-Xia, Yao Gen-Do
| [Analysis of common mutations of deafness-related genes in 2725 newborns].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Jun 32 (3): 335-8.
Yu Hong, Liu Dan, Yang Jingqun, Wu Zhiqiang, Sun Dongmei, Ma Wolo
| [Study of newborn hearing and genetic screening in Jinan].
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2015 May 50 (5): 401-5.
Xiang Lili, Lin Qian, Nie Wenying, Hou Qian, Li Hui, Li Yinghui, Liu Xinj
| GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness.
Cell biochemistry and biophysics 2015 Feb .
Fang Yuan, Gu Maosheng, Wang Chuanxia, Suo Feng, Wang Guangming, Xia Yuju
| Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population.
Journal of translational medicine 2015 13 263.
Kim So Young, Kim Ah Reum, Kim Nayoung K D, Kim Min Young, Jeon Eun-Hee, Kim Bong Jik, Han Young Eun, Chang Mun Young, Park Woong-Yang, Choi Byung Yo