185 related articles for article (PubMed ID: 19954013)
1. [Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China].
Yuan YY; Dai P; Zhu QW; Kang DY; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Jun; 44(6):449-54. PubMed ID: 19954013
[TBL] [Abstract][Full Text] [Related]
2. [Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].
Dai P; Yuan YY; Kang DY; Li Q; Zhu QW; Zhang X; Liu LX; Liu X; Huang DL
Zhonghua Yi Xue Za Zhi; 2007 Sep; 87(36):2521-5. PubMed ID: 18067822
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].
Li Q; Dai P; Huang DL; Yuan YY; Zhu QW; Han B; Liu X; Yu F; Kang DY; Zhang X; Xue DD; Jin ZC
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Dec; 42(12):893-7. PubMed ID: 18335745
[TBL] [Abstract][Full Text] [Related]
5. [Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7-2A to G mutation of the gene].
Li Q; Huang DL; Zhu QW; Yuan YY; Fang RP; Dai P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):610-5. PubMed ID: 21154317
[TBL] [Abstract][Full Text] [Related]
6. Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome.
Zhang F; Bai X; Xiao Y; Zhang X; Zhang G; Li J; Xu L; Wang H
Int J Pediatr Otorhinolaryngol; 2016 Jun; 85():75-9. PubMed ID: 27240500
[TBL] [Abstract][Full Text] [Related]
7. [Diagnostic function of SLC26A4 hot spot mutations screening to enlarged vestibular aqueduct syndrome].
Li Q; Fang R; You Y; Wang Y; Dai P
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Oct; 24(19):876-9. PubMed ID: 21174747
[TBL] [Abstract][Full Text] [Related]
8. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct.
Zhao X; Cheng X; Huang L; Wang X; Wen C; Wang X
Biosci Trends; 2018; 12(5):502-506. PubMed ID: 30473558
[TBL] [Abstract][Full Text] [Related]
9. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct.
Wang M; Zhang F; Xu L; Xiao Y; Li J; Fan Z; Sun Q; Bai X; Wang H
Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():170-174. PubMed ID: 27729126
[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. Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis.
Dai P; Yuan Y; Huang D; Zhu X; Yu F; Kang D; Yuan H; Wu B; Han D; Wong LJ
J Transl Med; 2008 Nov; 6():74. PubMed ID: 19040761
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome.
Chen K; Zhou W; Zong L; Liu M; Du J; Jiang H
Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1633-6. PubMed ID: 22906308
[TBL] [Abstract][Full Text] [Related]
15. [Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening].
Dai P; Zhu XH; Yuan YY; Zhu QW; Teng GC; Zhang X; Liu LX; Wang JL; Feng B; Zhai SQ; Kang DY; Liu X; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Jul; 41(7):497-500. PubMed ID: 17007371
[TBL] [Abstract][Full Text] [Related]
16. [The analysis of mutations in non-syndromic deafness gene SLC26A4 by next generation sequencing technology].
Chai F; Zhao HL; Han XD
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Apr; 33(4):357-361. PubMed ID: 30970410
[No Abstract] [Full Text] [Related]
17. Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
Hu H; Wu L; Feng Y; Pan Q; Long Z; Li J; Dai H; Xia K; Liang D; Niikawa N; Xia J
J Hum Genet; 2007; 52(6):492-497. PubMed ID: 17443271
[TBL] [Abstract][Full Text] [Related]
18. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct.
Yao G; Li S; Chen D; Wang H; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
Int J Pediatr Otorhinolaryngol; 2013 Apr; 77(4):544-9. PubMed ID: 23385134
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of genotypes and audiological characteristics of children with SLC26A4 gene pathogenic mutations].
Zhao XL; Huang LH; Wang XY; DU Y; Wang X; Cheng XH; Zhao LP; Li Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):836-840. PubMed ID: 29921053
[No Abstract] [Full Text] [Related]
20. Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis.
Lu YJ; Yao J; Wei QJ; Xing GQ; Cao X
Medicine (Baltimore); 2015 Dec; 94(50):e2248. PubMed ID: 26683941
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
