214 related articles for article (PubMed ID: 29798269)
1. [Autosomal dominant hearing loss resulting from mutation in the GJB2 gene:nonsyndromic presentation in a Chinese family].
Dai X; Li J; Hu XJ; Tong J; Cai WQ
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Dec; 30(24):1939-1941;1945. PubMed ID: 29798269
[No Abstract] [Full Text] [Related]
2. 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]
3. [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 Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2008 Jan; 22(1):14-7, 21. PubMed ID: 18338563
[TBL] [Abstract][Full Text] [Related]
4. R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.
Jiang SJ; Di ZH; Huang D; Zhang JB; Zhang YY; Li SQ; He R
Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1461-6. PubMed ID: 24975403
[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. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
Yuan YY; Dai P; Zhu XH; Kang DY; Zhang X; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr; 44(4):292-6. PubMed ID: 19558834
[TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant hearing loss resulting from p.R75Q mutation in the GJB2 gene: nonsyndromic presentation in a South Indian family.
Pavithra A; Selvakumari M; Nityaa V; Sharanya N; Ramakrishnan R; Narasimhan M; Srisailapathy CR
Ann Hum Genet; 2015 Jan; 79(1):76-82. PubMed ID: 25393658
[TBL] [Abstract][Full Text] [Related]
8. [Spectrum of
Zheng BJ; Zhang T; Wang H; Tang XW; Zheng J; Lv JX; Guan MX
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Jun; 30(12):933-937. PubMed ID: 29771057
[No Abstract] [Full Text] [Related]
9. 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]
10. Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children.
Hu X; Liang F; Zhao M; Gong A; Berry ER; Shi Y; Wang Y; Chen Y; Liu A; Qu C
Int J Pediatr Otorhinolaryngol; 2012 Oct; 76(10):1474-80. PubMed ID: 22796198
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
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. Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan.
Chu CW; Chen YJ; Lee YH; Jaung SJ; Lee FP; Huang HM
Int J Pediatr Otorhinolaryngol; 2015 Apr; 79(4):584-90. PubMed ID: 25724631
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 21055240
[TBL] [Abstract][Full Text] [Related]
16. [Molecular etiology of non-syndromic hearing impairment in a Chinese family].
Sun Q; Shan XZ; Ma LT; Kang DY; Zhang X; Liu X; Wang GJ; Yuan HJ; Han DY
Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2540-3. PubMed ID: 20137614
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.
Batissoco AC; Abreu-Silva RS; Braga MC; Lezirovitz K; Della-Rosa V; Alfredo T; Otto PA; Mingroni-Netto RC
Ear Hear; 2009 Feb; 30(1):1-7. PubMed ID: 19125024
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.
Utrera R; Ridaura V; Rodríguez Y; Rojas MJ; Mago L; Angeli S; Henríquez O
Genet Test; 2007; 11(4):347-52. PubMed ID: 18294049
[TBL] [Abstract][Full Text] [Related]
20. [Study of newborn hearing and genetic screening in Jinan].
Xiang L; Lin Q; Nie W; Hou Q; Li H; Li Y; Liu X
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 May; 50(5):401-5. PubMed ID: 26178053
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
