169 related articles for article (PubMed ID: 29871242)
1. [Analysis of deafness-related gene mutations in 23 nonsyndromic hearing impairment families in Guangxi Zhuang Autonomous Region].
Shi M; Liu F; Xu L; Liu M; Tang FZ; Liang JP; Lu QT; Zhai SH; Huang J; Chen RC
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Feb; 31(4):277-283. PubMed ID: 29871242
[No Abstract] [Full Text] [Related]
2. [Analysis common gene mutation spots of 127 non-syndromic deafness natients in Guangxi Drovince].
Liu S; Xu L; Chen B; Liu M; Qu S; Liang J; Tang F; Shi M; Peng L; Jing Y; Li F; Liang Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1954-8. PubMed ID: 26911057
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. [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]
6. 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. PubMed ID: 28583500
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.
Yang XL; Bai-Cheng X; Chen XJ; Pan-Pan B; Jian-Li M; Xiao-Wen L; Zhang ZW; Wan D; Zhu YM; Guo YF
Acta Otolaryngol; 2013 Sep; 133(9):930-4. PubMed ID: 23834103
[TBL] [Abstract][Full Text] [Related]
9. [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. PubMed ID: 21575411
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of the SLC26A4 mutation from 230 deafness patients in Guangxi region].
Liu M; Xu L; Tang FZ; Shi M; Qu SH; Liang JP; Lu QT; Chen RC; Huang J; Huang YY
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Oct; 30(19):1540-1544. PubMed ID: 29871136
[No Abstract] [Full Text] [Related]
11. A novel compound heterozygous mutation of SLC26A4 in two Chinese families with nonsyndromic hearing loss and enlarged vestibular aqueducts.
Zhu GJ; Shi LS; Zhou H; Yang Y; Chen J; Gao X
Mol Med Rep; 2017 Dec; 16(6):9011-9016. PubMed ID: 28990112
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal genetic test and clinical guidance for 213 hereditary deaf families].
Han MY; Lu YP; Bian XM; Wang LX; Huang SS; Wang GJ; Wang Y; Kang DY; Zhang X; Dai P
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Feb; 47(2):127-31. PubMed ID: 22455811
[TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.
Wang ZT; Chen Y; Chen DY; Chai YC; Pang XH; Sun LH; Wang XW; Yang T; Wu H
Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1513-6. PubMed ID: 25015771
[TBL] [Abstract][Full Text] [Related]
14. Variations in the Mutational Spectrum in Nonsyndromic Hearing Impairment: A study of the Special Schools for the Deaf in Southern China.
Lin Y; Yu F; Jiao Y; Zhou F
J Int Adv Otol; 2019 Aug; 15(2):247-252. PubMed ID: 31347505
[TBL] [Abstract][Full Text] [Related]
15. [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. PubMed ID: 25297579
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.
Morell RJ; Kim HJ; Hood LJ; Goforth L; Friderici K; Fisher R; Van Camp G; Berlin CI; Oddoux C; Ostrer H; Keats B; Friedman TB
N Engl J Med; 1998 Nov; 339(21):1500-5. PubMed ID: 9819448
[TBL] [Abstract][Full Text] [Related]
17. [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]
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. [Application of next generation sequencing in congenital sensorineural deafness].
Xu B; Chen Y; Jiang A; Chen C; Wang K; Zheng J; Fu Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):811-815. PubMed ID: 29921047
[No Abstract] [Full Text] [Related]
20. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
Kelley PM; Harris DJ; Comer BC; Askew JW; Fowler T; Smith SD; Kimberling WJ
Am J Hum Genet; 1998 Apr; 62(4):792-9. PubMed ID: 9529365
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]