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Results: 1 to 20 of 205

Similar articles for PubMed (Select 22991996)

1.

Identification of a p.R143Q dominant mutation in the gap junction beta-2 gene in three Chinese patients with different hearing phenotypes.

Huang S, Wang G, Xu Y, Yuan Y, Han D, Dai P.

Acta Otolaryngol. 2013 Jan;133(1):55-8. doi: 10.3109/00016489.2012.715373. Epub 2012 Sep 19. Erratum in: Acta Otolaryngol. 2013 Jun;133(6):672.

PMID:
22991996
2.

De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss.

Huang S, Yuan Y, Liu J, Han D, Kang D, Zhang X, Dong M, Yan X, Dai P.

Int J Pediatr Otorhinolaryngol. 2011 Oct;75(10):1333-6. doi: 10.1016/j.ijporl.2011.07.033. Epub 2011 Aug 24.

PMID:
21868108
3.

R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.

Jiang SJ, Di ZH, Huang D, Zhang JB, Zhang YY, Li SQ, He R.

Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1461-6. doi: 10.1016/j.ijporl.2014.06.008. Epub 2014 Jun 16.

PMID:
24975403
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. Chinese.

PMID:
23141447
5.

Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.

Yuan Y, Yu F, Wang G, Huang S, Yu R, Zhang X, Huang D, Han D, Dai P.

J Transl Med. 2010 Dec 2;8:127. doi: 10.1186/1479-5876-8-127.

6.

Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese family.

Huang A, Yuan Y, Duan N, Jiang X, Wang B, Liu Y, Kang D, Zhang X, Zhu Q, Dai P.

Int J Pediatr Otorhinolaryngol. 2014 Apr;78(4):599-603. doi: 10.1016/j.ijporl.2014.01.008. Epub 2014 Jan 17.

PMID:
24503448
7.

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 10;7:79. doi: 10.1186/1479-5876-7-79.

8.

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. doi: 10.3892/mmr.2014.2148. Epub 2014 Apr 15.

PMID:
24737404
9.
10.

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 4;11:163. doi: 10.1186/1479-5876-11-163.

11.

[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances].

Lalaiants MR, Markova TG, Bakhshinian VV, Bliznets EA, Poliakov AV, Tavartikiladze GA.

Vestn Otorinolaringol. 2014;(2):37-43. Russian.

PMID:
24781170
12.

Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes.

Huang S, Han D, Wang G, Yuan Y, Song Y, Han M, Chen Z, Dai P.

Int J Pediatr Otorhinolaryngol. 2013 Mar;77(3):379-83. doi: 10.1016/j.ijporl.2012.11.031. Epub 2012 Dec 21.

PMID:
23266159
13.

Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: further confirmation of pathogenicity and haplotype analysis in Asian populations.

Gallant E, Francey L, Tsai EA, Berman M, Zhao Y, Fetting H, Kaur M, Deardorff MA, Wilkens A, Clark D, Hakonarson H, Rehm HL, Krantz ID.

Am J Med Genet A. 2013 Sep;161A(9):2148-57. doi: 10.1002/ajmg.a.36042. Epub 2013 Jul 19.

14.

[Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].

Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):367-73. doi: 10.3760/cma.j.issn.1003-9406.2011.04.002. Chinese.

PMID:
21811972
15.

[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 Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 May;25(10):445-8. Chinese.

PMID:
21809555
16.

Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.

Ben Said M, Dhouib H, BenZina Z, Ghorbel A, Moreno F, Masmoudi S, Ayadi H, Hmani-Aifa M.

Int J Pediatr Otorhinolaryngol. 2012 Jun;76(6):832-6. doi: 10.1016/j.ijporl.2012.02.053. Epub 2012 Mar 18.

PMID:
22429511
17.

Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 gene.

Zhao FF, Ji YB, Wang DY, Lan L, Han MK, Li Q, Zhao Y, Rao S, Han D, Wang QJ.

Genet Test Mol Biomarkers. 2011 Sep;15(9):619-25. doi: 10.1089/gtmb.2010.0192. Epub 2011 Apr 13.

PMID:
21488715
18.

GJB2 allele variants and the associated audiologic features identified in Chinese patients with less severe idiopathic hearing loss.

Zhang J, Wang Z, Dai W, Zeng Y, Li H.

Genet Test Mol Biomarkers. 2011 May;15(5):313-8. doi: 10.1089/gtmb.2010.0182. Epub 2011 Mar 2.

PMID:
21366436
19.

Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.

Riahi Z, Zainine R, Mellouli Y, Hannachi R, Bouyacoub Y, Laroussi N, Beltaief N, Kefi R, Romdhane L, Bonnet C, Abdelhak S, Besbes G.

Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1481-4. doi: 10.1016/j.ijporl.2013.06.013. Epub 2013 Jul 12. Review.

PMID:
23856378
20.

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. doi: 10.3109/00016489.2010.483479. Epub 2010 Dec 16.

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