205 related articles for article (PubMed ID: 30973918)
1. 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]
2. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang YB; Tang SH; Li HZ; Xu CY; Chen C; Xu YZ; Ding LR; Xu XQ
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():185-190. PubMed ID: 31035178
[TBL] [Abstract][Full Text] [Related]
3. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.
Hu H; Zhou P; Wu J; Lei W; Wang Y; Yang Y; Liu H
Medicine (Baltimore); 2021 Apr; 100(17):e25647. PubMed ID: 33907123
[TBL] [Abstract][Full Text] [Related]
6. 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]
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; 7():79. PubMed ID: 19744334
[TBL] [Abstract][Full Text] [Related]
8. 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; 12():64. PubMed ID: 24612839
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. 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]
12. Prevalence of mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 genes in 103 children with sensorineural hearing loss in Shaoxing, China.
Yu H; Liu D; Yang J; Wu Z
Ear Nose Throat J; 2018 Jun; 97(6):E33-E38. PubMed ID: 30036422
[TBL] [Abstract][Full Text] [Related]
13. [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. PubMed ID: 25297577
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.
Xiong Y; Chen M; Wang H; Chen L; Huang H; Xu L
Int J Pediatr Otorhinolaryngol; 2024 Jan; 176():111777. PubMed ID: 38029595
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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. PubMed ID: 24737404
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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; 11():163. PubMed ID: 23826813
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
