98 related articles for article (PubMed ID: 26004784)
1. 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. PubMed ID: 26004784
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 28640090
[TBL] [Abstract][Full Text] [Related]
3. [A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss].
Zhang D; Duan H; Lin P; Cheng J; Wang C; Ma Y; Cheng Y; Zhao H; Wang W; Xu K; Han D; Yuan H
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Mar; 51(3):203-8. PubMed ID: 27033575
[TBL] [Abstract][Full Text] [Related]
4. A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.
Du W; Cheng J; Ding H; Jiang Z; Guo Y; Yuan H
Genomics; 2014 Oct; 104(4):264-70. PubMed ID: 25149764
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 25761933
[TBL] [Abstract][Full Text] [Related]
6. Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
Zhang F; Xiao Y; Xu L; Zhang X; Zhang G; Li J; Lv H; Bai X; Wang H
Biomed Res Int; 2016; 2016():1302914. PubMed ID: 27247933
[TBL] [Abstract][Full Text] [Related]
7. A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss.
Liu Y; Hu C; Liu C; Liu D; Mei L; He C; Jiang L; Wu H; Chen H; Feng Y
PLoS One; 2019; 14(4):e0215212. PubMed ID: 30973918
[TBL] [Abstract][Full Text] [Related]
8. Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.
Gao Z; Lu Y; Ke J; Li T; Hu P; Song Y; Xu C; Wang J; Cheng J; Zhang L; Duan H; Yuan H; Ma F
PLoS One; 2016; 11(10):e0165650. PubMed ID: 27792752
[TBL] [Abstract][Full Text] [Related]
9. 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; 11():312. PubMed ID: 24341454
[TBL] [Abstract][Full Text] [Related]
10. Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.
Li Q; Ji Y; Han B; Zong L; Lan L; Zhao Y; Wang H; Wang D; Wang Q
Chin Med J (Engl); 2014; 127(18):3233-7. PubMed ID: 25266519
[TBL] [Abstract][Full Text] [Related]
11. A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China.
Ming L; Wang Y; Lu W; Sun T
Genet Test Mol Biomarkers; 2019 Jan; 23(1):51-56. PubMed ID: 30589569
[TBL] [Abstract][Full Text] [Related]
12. [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 Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1959-62. PubMed ID: 26911058
[TBL] [Abstract][Full Text] [Related]
13. Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing.
Zhao P; Lin L; Lan L
Medicine (Baltimore); 2018 Sep; 97(38):e12285. PubMed ID: 30235673
[TBL] [Abstract][Full Text] [Related]
14. [Epidemiological analysis of GJB2,SLC26A4,mtRNA,GJB3 in nonsyndromic hearing loss in Kashi in Xinjiang].
Sun J; Chen Y; Zhang H; Wen H
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Apr; 31(8):619-622. PubMed ID: 29871328
[No Abstract] [Full Text] [Related]
15. 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; 8(8):e68692. PubMed ID: 23990876
[TBL] [Abstract][Full Text] [Related]
16. Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.
Duan SH; Ma JL; Yang XL; Guo YF
Mol Med Rep; 2017 Nov; 16(5):6722-6728. PubMed ID: 28901477
[TBL] [Abstract][Full Text] [Related]
17. A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population.
Sagong B; Baek JI; Oh SK; Na KJ; Bae JW; Choi SY; Jeong JY; Choi JY; Lee SH; Lee KY; Kim UK
PLoS One; 2013; 8(3):e57237. PubMed ID: 23469187
[TBL] [Abstract][Full Text] [Related]
18. [A new method for simultaneous multi-gene mutation screening in 355 patients with nonsyndromic hearing loss of Inner Mongolia Autonomous region].
Zhang D; Duan H; Yuan H; Han D
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1941-6. PubMed ID: 26911054
[TBL] [Abstract][Full Text] [Related]
19. [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. PubMed ID: 19199245
[TBL] [Abstract][Full Text] [Related]
20. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India.
Adhikary B; Ghosh S; Paul S; Bankura B; Pattanayak AK; Biswas S; Maity B; Das M
Gene; 2015 Dec; 573(2):239-45. PubMed ID: 26188157
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
