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Items: 1 to 20 of 100

1.

Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants.

Du W, Zhu YM, Guo YF, Wang QJ, Liu XW.

Acta Otolaryngol. 2014 Apr;134(4):373-81. doi: 10.3109/00016489.2013.849817. Epub 2013 Nov 21.

PMID:
24256046
2.

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
3.

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. doi: 10.1097/MAO.0b013e3181e3d324.

PMID:
20601923
4.

Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.

Popova DP, Kaneva R, Varbanova S, Popov TM.

Eur Arch Otorhinolaryngol. 2012 Jun;269(6):1589-92. doi: 10.1007/s00405-011-1817-2. Epub 2011 Oct 29.

PMID:
22037723
5.

A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.

Riahi Z, Chahed H, Jaafoura H, Zainine R, Messaoud O, Naili M, Nagara M, Hammami H, Laroussi N, Bouyacoub Y, Kefi R, Bonnet C, Besbes G, Abdelhak S.

Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1485-8. doi: 10.1016/j.ijporl.2013.06.015. Epub 2013 Jul 12.

PMID:
23856379
6.

[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
7.

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

Dai P, Yu F, Han B, Wu H, Yuan YY, Li Q, Wang GJ, Liu X, He J, Huang DL, Kang DY, Zhang X, Yuan HJ, Leejun CW, Han DY.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):804-8. Chinese.

PMID:
18300439
8.

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ.

JAMA. 1999 Jun 16;281(23):2211-6.

PMID:
10376574
9.

[High prevalence of connexin-26 (GJB2) mutation in cochlear implant recipients].

Chen DY, Chen XW, Cao KL, Jin X, Zuo J, Wei CG, Fang FD.

Zhonghua Yi Xue Za Zhi. 2006 Nov 28;86(44):3114-7. Chinese.

PMID:
17313762
10.

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.

11.

Connexin gene mutations among Ugandan patients with nonsyndromic sensorineural hearing loss.

Javidnia H, Carson N, Awubwa M, Byaruhanga R, Mack D, Vaccani JP.

Laryngoscope. 2014 Sep;124(9):E373-6. doi: 10.1002/lary.24697. Epub 2014 May 2.

PMID:
24706568
12.

[Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)].

Barashkov NA, Dzhemileva LU, Fedorova SA, Maksimova NR, Khusnutdinova EK.

Vestn Otorinolaringol. 2008;(5):23-8. Russian.

PMID:
19008837
13.

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB.

Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8.

PMID:
12176179
14.

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

Dai P, Yu F, Han B, Yuan Y, Li Q, Wang G, Liu X, He J, Huang D, Kang D, Zhang X, Yuan H, Schmitt E, Han D, Wong LJ.

Genet Med. 2007 May;9(5):283-9.

PMID:
17505205
15.

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.

16.

[Mutation analysis of GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city].

Yuan Y, Huang D, Dai P, Zhu X, Yu F, Zhang X, Liu L, Han D.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 Jan;22(1):14-7, 21. Chinese.

PMID:
18338563
17.

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. doi: 10.1089/gtmb.2014.0241.

18.

[Study on nonsyndromic hereditary hearing impairment mutations of GJB2 gene in Uyghur patients in Xinjiang].

Li Y, Guan H, Xu H, Li H, Li H, Wei Y, Ya S, Gong J.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jul;24(13):604-7, 612. Chinese.

PMID:
20842950
19.

[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases].

Yu F, Han DY, Dai P, Kang DY, Zhang X, Liu X, Zhu QW, Yuan YY, Sun Q, Xue DD, Li M, Liu J, Yuan HJ, Yang WY.

Zhonghua Yi Xue Za Zhi. 2007 Oct 30;87(40):2814-9. Chinese.

PMID:
18167282
20.

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