278 related articles for article (PubMed ID: 28583500)
1. 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]
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. [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]
4. [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]
5. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
Huang B; Han M; Wang G; Huang S; Zeng J; Yuan Y; Dai P
Int J Pediatr Otorhinolaryngol; 2018 May; 108():49-54. PubMed ID: 29605365
[TBL] [Abstract][Full Text] [Related]
6. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.
Duan SH; Zhu YM; Wang YL; Guo YF
Acta Otolaryngol; 2015 Jun; 135(6):586-91. PubMed ID: 25761933
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Zhou Y; Li C; Li M; Zhao Z; Tian S; Xia H; Liu P; Han Y; Ren R; Chen J; Jia C; Guo W
Mol Genet Genomic Med; 2019 Mar; 7(3):e537. PubMed ID: 30693673
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of GJB2, SLC26A4, GJB3 and 12S rRNA gene mutations among patients with nonsyndromic hearing loss from eastern Shandong].
Sun S; Niu L; Tian J; Chen W; Li Y; Xia N; Jyu C; Chen X; Zhang C; Lan X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):433-438. PubMed ID: 31030427
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Analysis of common mutations of deafness-related genes in 2725 newborns].
Yu H; Liu D; Yang J; Wu Z; Sun D; Ma W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):335-8. PubMed ID: 26037344
[TBL] [Abstract][Full Text] [Related]
13. GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.
Ma Y; Xiao Y; Bai X; Zhang F; Zhang D; Xu X; Xu L; Wang H
Acta Otolaryngol; 2016 Aug; 136(8):800-5. PubMed ID: 27066914
[TBL] [Abstract][Full Text] [Related]
14. Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.
Xin F; Yuan Y; Deng X; Han M; Wang G; Zhao J; Gao X; Liu J; Yu F; Han D; Dai P
J Transl Med; 2013 Dec; 11():312. PubMed ID: 24341454
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array.
He X; Li X; Guo Y; Zhao Y; Dong H; Dong J; Zhong L; Shi Z; Zhang Y; Soliman M; Song C; Zhao Z
Am J Audiol; 2018 Mar; 27(1):57-66. PubMed ID: 29234782
[TBL] [Abstract][Full Text] [Related]
17. Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.
Yang XL; Bai-Cheng X; Chen XJ; Pan-Pan B; Jian-Li M; Xiao-Wen L; Zhang ZW; Wan D; Zhu YM; Guo YF
Acta Otolaryngol; 2013 Sep; 133(9):930-4. PubMed ID: 23834103
[TBL] [Abstract][Full Text] [Related]
18. [Common gene mutations study in Uyghur population with deafness in Kashgar region of Xinjiang].
Chen Y; Tudi M; Lu HL; Jiang D; Zhao J; Hu B; Kuyaxi P; Zhang H
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Mar; 46(3):205-8. PubMed ID: 21575411
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.
Duan SH; Ma JL; Yang XL; Guo YF
Mol Med Rep; 2017 Nov; 16(5):6722-6728. PubMed ID: 28901477
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]