209 related articles for article (PubMed ID: 27247933)
1. Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
Zhang F; Xiao Y; Xu L; Zhang X; Zhang G; Li J; Lv H; Bai X; Wang H
Biomed Res Int; 2016; 2016():1302914. PubMed ID: 27247933
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India.
Adhikary B; Ghosh S; Paul S; Bankura B; Pattanayak AK; Biswas S; Maity B; Das M
Gene; 2015 Dec; 573(2):239-45. PubMed ID: 26188157
[TBL] [Abstract][Full Text] [Related]
4. A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.
Du W; Cheng J; Ding H; Jiang Z; Guo Y; Yuan H
Genomics; 2014 Oct; 104(4):264-70. PubMed ID: 25149764
[TBL] [Abstract][Full Text] [Related]
5. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
Yuan YY; Dai P; Zhu XH; Kang DY; Zhang X; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr; 44(4):292-6. PubMed ID: 19558834
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss.
Han R; Li L; Duan L; Xia Y; Kuyaxi P; Zhao J; Zhao Q; Zhang H; Chen Y
Medicine (Baltimore); 2017 Jun; 96(25):e7149. PubMed ID: 28640090
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.
Li H; Wang B; Liu D; Wang T; Li Q; Wang W; Li H
Genomics; 2015 Aug; 106(2):83-7. PubMed ID: 26004784
[TBL] [Abstract][Full Text] [Related]
11. [A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss].
Zhang D; Duan H; Lin P; Cheng J; Wang C; Ma Y; Cheng Y; Zhao H; Wang W; Xu K; Han D; Yuan H
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Mar; 51(3):203-8. PubMed ID: 27033575
[TBL] [Abstract][Full Text] [Related]
12. Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.
Zhang M; Han Y; Zhang F; Bai X; Wang H
Acta Otolaryngol; 2019 Jul; 139(7):612-617. PubMed ID: 31107121
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. [Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography].
Zhao J; Wu LQ; Feng Y; Pan Q; Zhao K; Li HY; Liang DS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):21-5. PubMed ID: 19199245
[TBL] [Abstract][Full Text] [Related]
16. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P
PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218
[TBL] [Abstract][Full Text] [Related]
17. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.
Tsukada K; Nishio SY; Hattori M; Usami S
Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1():61S-76S. PubMed ID: 25999548
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].
Wang G; Yuan Y; Li R; Han M; Huang S; Kang D; Zhang X; Dong M; Dai P; Han D
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 May; 25(10):445-8. PubMed ID: 21809555
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]