277 related articles for article (PubMed ID: 30589569)
1. A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China.
Ming L; Wang Y; Lu W; Sun T
Genet Test Mol Biomarkers; 2019 Jan; 23(1):51-56. PubMed ID: 30589569
[TBL] [Abstract][Full Text] [Related]
2. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang YB; Tang SH; Li HZ; Xu CY; Chen C; Xu YZ; Ding LR; Xu XQ
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():185-190. PubMed ID: 31035178
[TBL] [Abstract][Full Text] [Related]
3. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
[TBL] [Abstract][Full Text] [Related]
4. [Epidemiological analysis of GJB2,SLC26A4,mtRNA,GJB3 in nonsyndromic hearing loss in Kashi in Xinjiang].
Sun J; Chen Y; Zhang H; Wen H
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Apr; 31(8):619-622. PubMed ID: 29871328
[No Abstract] [Full Text] [Related]
5. [Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].
Yang A; Geng M; Zhang H; Guo X; Tang J; Han F
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1959-62. PubMed ID: 26911058
[TBL] [Abstract][Full Text] [Related]
6. Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.
Jiang H; Chen J; Shan XJ; Li Y; He JG; Yang BB
Mol Med Rep; 2014 Jul; 10(1):379-86. PubMed ID: 24737404
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.
Yuan Y; You Y; Huang D; Cui J; Wang Y; Wang Q; Yu F; Kang D; Yuan H; Han D; Dai P
J Transl Med; 2009 Sep; 7():79. PubMed ID: 19744334
[TBL] [Abstract][Full Text] [Related]
8. Prevalence of mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 genes in 103 children with sensorineural hearing loss in Shaoxing, China.
Yu H; Liu D; Yang J; Wu Z
Ear Nose Throat J; 2018 Jun; 97(6):E33-E38. PubMed ID: 30036422
[TBL] [Abstract][Full Text] [Related]
9. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
Ji YB; Han DY; Lan L; Wang DY; Zong L; Zhao FF; Liu Q; Benedict-Alderfer C; Zheng QY; Wang QJ
Acta Otolaryngol; 2011 Feb; 131(2):124-9. PubMed ID: 21162657
[TBL] [Abstract][Full Text] [Related]
10. Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children.
Hu X; Liang F; Zhao M; Gong A; Berry ER; Shi Y; Wang Y; Chen Y; Liu A; Qu C
Int J Pediatr Otorhinolaryngol; 2012 Oct; 76(10):1474-80. PubMed ID: 22796198
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].
Wang YL; Zhu YM; Liu XW; Xu BC; Guo YF; Wang QJ
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 47(9):760-3. PubMed ID: 23141447
[TBL] [Abstract][Full Text] [Related]
12. Microarray-based mutation detection of pediatric sporadic nonsyndromic hearing loss in China.
Qu C; Sun X; Shi Y; Gong A; Liang S; Zhao M; Chen Y; Liang F
Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):235-9. PubMed ID: 22154049
[TBL] [Abstract][Full Text] [Related]
13. Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
Wei Q; Wang S; Yao J; Lu Y; Chen Z; Xing G; Cao X
J Transl Med; 2013 Jul; 11():163. PubMed ID: 23826813
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.
Pan J; Xu P; Tang W; Cui Z; Feng M; Wang C
Int J Pediatr Otorhinolaryngol; 2017 Jul; 98():39-42. PubMed ID: 28583500
[TBL] [Abstract][Full Text] [Related]
15. Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum.
Chen K; Zong L; Liu M; Wang X; Zhou W; Zhan Y; Cao H; Dong C; Tang H; Jiang H
J Transl Med; 2014 Mar; 12():64. PubMed ID: 24612839
[TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.
Xiong Y; Chen M; Wang H; Chen L; Huang H; Xu L
Int J Pediatr Otorhinolaryngol; 2024 Jan; 176():111777. PubMed ID: 38029595
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
Luo J; Bai X; Zhang F; Xiao Y; Gu L; Han Y; Fan Z; Li J; Xu L; Wang H
Ann Hum Genet; 2017 Nov; 81(6):258-266. PubMed ID: 28786104
[TBL] [Abstract][Full Text] [Related]
18. Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss.
Yao G; Chen D; Wang H; Li S; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
Acta Otolaryngol; 2013 Aug; 133(8):833-41. PubMed ID: 23638949
[TBL] [Abstract][Full Text] [Related]
19. [Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis].
Lyu K; Xiong Y; Yu H; Zou L; Ran L; Liu D; Yin Q; Xu Y; Fang X; Song Z; Huang L; Tan D; Zhang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):547-52. PubMed ID: 25297577
[TBL] [Abstract][Full Text] [Related]
20. Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing.
Zhao P; Lin L; Lan L
Medicine (Baltimore); 2018 Sep; 97(38):e12285. PubMed ID: 30235673
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]