179 related articles for article (PubMed ID: 27018795)
1. Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.
Wu H; Feng Y; Jiang L; Pan Q; Liu Y; Liu C; He C; Chen H; Liu X; Hu C; Hu Y; Mei L
PLoS One; 2016; 11(3):e0151909. PubMed ID: 27018795
[TBL] [Abstract][Full Text] [Related]
2. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Albert S; Blons H; Jonard L; Feldmann D; Chauvin P; Loundon N; Sergent-Allaoui A; Houang M; Joannard A; Schmerber S; Delobel B; Leman J; Journel H; Catros H; Dollfus H; Eliot MM; David A; Calais C; Drouin-Garraud V; Obstoy MF; Tran Ba Huy P; Lacombe D; Duriez F; Francannet C; Bitoun P; Petit C; Garabédian EN; Couderc R; Marlin S; Denoyelle F
Eur J Hum Genet; 2006 Jun; 14(6):773-9. PubMed ID: 16570074
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. [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]
8. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct.
He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Chang J; Xie M; Zhong B; Lu X
Int J Pediatr Otorhinolaryngol; 2017 Apr; 95():104-108. PubMed ID: 28576516
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
Huang S; Han D; Yuan Y; Wang G; Kang D; Zhang X; Yan X; Meng X; Dong M; Dai P
J Transl Med; 2011 Sep; 9():167. PubMed ID: 21961810
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.
Wang ZT; Chen Y; Chen DY; Chai YC; Pang XH; Sun LH; Wang XW; Yang T; Wu H
Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1513-6. PubMed ID: 25015771
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct.
Lai R; Hu P; Zhu F; Zhu G; Vivero R; Peng A; Wu W; Xiao Z; Liu X; Xie D
J Laryngol Otol; 2012 Apr; 126(4):349-55. PubMed ID: 22289209
[TBL] [Abstract][Full Text] [Related]
17. SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.
Dai P; Li Q; Huang D; Yuan Y; Kang D; Miller DT; Shao H; Zhu Q; He J; Yu F; Liu X; Han B; Yuan H; Platt OS; Han D; Wu BL
Genet Med; 2008 Aug; 10(8):586-92. PubMed ID: 18641518
[TBL] [Abstract][Full Text] [Related]
18. Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.
Chen S; Dong C; Wang Q; Zhong Z; Qi Y; Ke X; Liu Y
Genet Test Mol Biomarkers; 2016 Nov; 20(11):660-665. PubMed ID: 27610647
[TBL] [Abstract][Full Text] [Related]
19. Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.
de Moraes VC; dos Santos NZ; Ramos PZ; Svidnicki MC; Castilho AM; Sartorato EL
Int J Pediatr Otorhinolaryngol; 2013 Mar; 77(3):410-3. PubMed ID: 23273637
[TBL] [Abstract][Full Text] [Related]
20. Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study.
Miyagawa M; Nishio SY; Usami S;
J Hum Genet; 2014 May; 59(5):262-8. PubMed ID: 24599119
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
