Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 151

1.

Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.

Choi BY, Park G, Gim J, Kim AR, Kim BJ, Kim HS, Park JH, Park T, Oh SH, Han KH, Park WY.

PLoS One. 2013 Aug 22;8(8):e68692. doi: 10.1371/journal.pone.0068692. eCollection 2013.

2.

Strategy for the customized mass screening of genetic sensorineural hearing loss in koreans.

Chang MY, Choi BY.

Korean J Audiol. 2014 Sep;18(2):45-9. doi: 10.7874/kja.2014.18.2.45. Epub 2014 Sep 16. Review.

3.

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.

4.

[Analysis and prenatal diagnosis of deafness-related gene mutations in patients with nonsyndromic hearing loss].

Li H, Chen Y, Mao Y, Ding Y, Xu X, Tang S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):553-6. doi: 10.3760/cma.j.issn.1003-9406.2014.01.002. Chinese.

PMID:
25297579
5.
6.

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.

7.

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
8.

[Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].

Yang A, Geng M, Zhang H, Guo X, Tang J, Han F.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Nov;29(22):1959-62. Chinese.

PMID:
26911058
9.

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.

10.

Spectrum of GJB2 mutations in a cohort of nonsyndromic hearing loss cases from the Kingdom of Saudi Arabia.

Al-Qahtani MH, Baghlab I, Chaudhary AG, Abuzenadah AM, Bamanie A, Daghistani KJ, Safieh M, Fida L, Dallol A.

Genet Test Mol Biomarkers. 2010 Feb;14(1):79-83. doi: 10.1089/gtmb.2009.0111.

PMID:
19929407
11.

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.

Li H, Wang B, Liu D, Wang T, Li Q, Wang W, Li H.

Genomics. 2015 Aug;106(2):83-7. doi: 10.1016/j.ygeno.2015.05.004. Epub 2015 May 22.

PMID:
26004784
12.

[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
13.

Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations.

Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li H.

Clin Genet. 2015 Jun;87(6):588-93. doi: 10.1111/cge.12431. Epub 2014 Aug 7.

PMID:
24853665
14.

[Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography].

Zhao J, Wu LQ, Feng Y, Pan Q, Zhao K, Li HY, Liang DS.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):21-5. doi: 10.3760/cma.j.issn.1003-9406.2009.01.005. Chinese.

PMID:
19199245
15.

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China.

Xu BC, Bian PP, Liu XW, Zhu YM, Yang XL, Ma JL, Chen XJ, Wang YL, Guo YF.

Acta Otolaryngol. 2014 Sep;134(9):924-9. doi: 10.3109/00016489.2014.927588. Epub 2014 Jun 18.

PMID:
24941117
16.

[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].

Dai P, Yu F, Kang DY, Zhang X, Liu X, Mi WZ, Cao JY, Yuan HJ, Yang WY, Wu BL, Han DY.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Oct;40(10):769-73. Chinese.

PMID:
16408730
17.

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
18.

[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
19.

Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss.

Han R, Li L, Duan L, Xia Y, Kuyaxi P, Zhao J, Zhao Q, Zhang H, Chen Y.

Medicine (Baltimore). 2017 Jun;96(25):e7149. doi: 10.1097/MD.0000000000007149.

20.

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

Supplemental Content

Support Center