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Items: 1 to 20 of 309

1.

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 14;9:154. doi: 10.1186/1479-5876-9-154.

2.

[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. doi: 10.3760/cma.j.issn.1003-9406.2014.05.001. Chinese.

PMID:
25297577
3.

[Common gene mutations study in Uyghur population with deafness in Kashgar region of Xinjiang].

Chen Y, Tudi M, Lu HL, Jiang D, Zhao J, Hu B, Kuyaxi P, Zhang H.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Mar;46(3):205-8. Chinese.

PMID:
21575411
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.

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 17;11:312. doi: 10.1186/1479-5876-11-312.

6.

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.

Duan SH, Zhu YM, Wang YL, Guo YF.

Acta Otolaryngol. 2015 Jun;135(6):586-91. doi: 10.3109/00016489.2015.1006334. Epub 2015 Mar 11.

PMID:
25761933
7.

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 11;12:64. doi: 10.1186/1479-5876-12-64.

8.

Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.

Du W, Wang Q, Zhu Y, Wang Y, Guo Y.

Biomed Res Int. 2014;2014:746838. doi: 10.1155/2014/746838. Epub 2014 Apr 2.

9.

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
10.

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. doi: 10.1016/j.ijporl.2017.04.018. Epub 2017 Apr 12.

PMID:
28583500
11.

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. doi: 10.1097GIM.0b013e31817d2ef1.

PMID:
18641518
12.

[Application of MALDI-TOF-MS in gene testing for non-syndromic hearing loss].

Zeng Y, Jiang D, Feng DF, Jin DD, Wu XH, Ding YL, Zou J.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):985-90. Chinese.

PMID:
24506996
13.

[Comparative analysis of the recurrent mutations between Uigur and Han ethnic deaf group in Xinjiang region of China].

Li Q, Fang R, Huang D, Wang G, Liu X, Dai P.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jan;24(1):11-5. Chinese.

PMID:
20235449
14.

[Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China].

Li Q, Dai P, Huang DL, Zhang J, Wang GJ, Zhu QW, Liu X, Han DY.

Zhonghua Yi Xue Za Zhi. 2007 Nov 13;87(42):2977-81. Chinese.

PMID:
18261328
15.

[Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].

Li YH, Jiang H, Yang LJ, Xu HX, Li H, Li HW, Luo YH, Wang CW, Zou GH.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Aug;45(8):645-51. Chinese.

PMID:
21055240
16.

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ.

Acta Otolaryngol. 2008 Mar;128(3):297-303. doi: 10.1080/00016480701767382.

PMID:
18274916
17.
18.

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.

19.

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss.

Zheng J, Ying Z, Cai Z, Sun D, He Z, Gao Y, Zhang T, Zhu Y, Chen Y, Guan MX.

PLoS One. 2015 Jun 4;10(6):e0128691. doi: 10.1371/journal.pone.0128691. eCollection 2015.

20.

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.

Ma Y, Xiao Y, Bai X, Zhang F, Zhang D, Xu X, Xu L, Wang H.

Acta Otolaryngol. 2016 Aug;136(8):800-5. doi: 10.3109/00016489.2016.1164893. Epub 2016 Apr 12.

PMID:
27066914

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