141 related articles for article (PubMed ID: 21387690)
1. [Molecular diagnosis of deafness].
Usami S
Nihon Rinsho; 2011 Feb; 69(2):357-67. PubMed ID: 21387690
[TBL] [Abstract][Full Text] [Related]
2. The responsible genes in Japanese deafness patients and clinical application using Invader assay.
Usami S; Wagatsuma M; Fukuoka H; Suzuki H; Tsukada K; Nishio S; Takumi Y; Abe S
Acta Otolaryngol; 2008 Apr; 128(4):446-54. PubMed ID: 18368581
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
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. 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]
7. 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]
8. [Analysis of common mutations of deafness-related genes in 2725 newborns].
Yu H; Liu D; Yang J; Wu Z; Sun D; Ma W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):335-8. PubMed ID: 26037344
[TBL] [Abstract][Full Text] [Related]
9. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
Huang B; Han M; Wang G; Huang S; Zeng J; Yuan Y; Dai P
Int J Pediatr Otorhinolaryngol; 2018 May; 108():49-54. PubMed ID: 29605365
[TBL] [Abstract][Full Text] [Related]
10. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
[TBL] [Abstract][Full Text] [Related]
11. Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.
Han B; Zong L; Li Q; Zhang Z; Wang D; Lan L; Zhang J; Zhao Y; Wang Q
Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1440-5. PubMed ID: 23815884
[TBL] [Abstract][Full Text] [Related]
12. GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness.
Fang Y; Gu M; Wang C; Suo F; Wang G; Xia Y
Cell Biochem Biophys; 2015 Sep; 73(1):41-4. PubMed ID: 25649612
[TBL] [Abstract][Full Text] [Related]
13. Suspension array-based deafness genetic screening in 53,033 Chinese newborns identifies high prevalence of 109 G>A in GJB2.
Zou Y; Dai QQ; Tao WJ; Wen XL; Feng DF; Deng H; Zhou WP; Li M; Zhang L
Int J Pediatr Otorhinolaryngol; 2019 Nov; 126():109630. PubMed ID: 31442870
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.
Hutchin T; Coy NN; Conlon H; Telford E; Bromelow K; Blaydon D; Taylor G; Coghill E; Brown S; Trembath R; Liu XZ; Bitner-Glindzicz M; Mueller R
Clin Genet; 2005 Dec; 68(6):506-12. PubMed ID: 16283880
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.
Usami S; Nishio SY; Nagano M; Abe S; Yamaguchi T;
PLoS One; 2012; 7(2):e31276. PubMed ID: 22384008
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns].
Sun X; Xi Z; Zhang J; Liu B; Xing X; Huang X; Zhao Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):766-70. PubMed ID: 26663044
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
