401 related articles for article (PubMed ID: 24737404)
1. 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]
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. 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]
4. 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]
5. [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]
6. 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]
7. 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]
8. [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]
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. Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
Qing J; Zhou Y; Lai R; Hu P; Ding Y; Wu W; Xiao Z; Ho PT; Liu Y; Liu J; Du L; Yan D; Goldstein BJ; Liu X; Xie D
Genet Test Mol Biomarkers; 2015 Jan; 19(1):52-8. PubMed ID: 25493717
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. 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]
14. Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study.
Chen Y; Tudi M; Sun J; He C; Lu HL; Shang Q; Jiang D; Kuyaxi P; Hu B; Zhang H
J Transl Med; 2011 Sep; 9():154. PubMed ID: 21917135
[TBL] [Abstract][Full Text] [Related]
15. Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation.
Chen K; Wang X; Sun L; Jiang H
Otolaryngol Head Neck Surg; 2012 Jun; 146(6):972-8. PubMed ID: 22412181
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. 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]
19. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.
Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM
Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]