These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
229 related articles for article (PubMed ID: 27308839)
21. Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China. Zhang J; Wang P; Han B; Ding Y; Pan L; Zou J; Liu H; Pang X; Liu E; Wang H; Liu H; Zhang X; Cheng X; Feng D; Li Q; Wang D; Zong L; Yi Y; Tian N; Mu F; Tian G; Chen Y; Liu G; Zhang F; Yi X; Yang L; Wang Q Int J Pediatr Otorhinolaryngol; 2013 Dec; 77(12):1929-35. PubMed ID: 24100002 [TBL] [Abstract][Full Text] [Related]
22. Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening. Schimmenti LA; Warman B; Schleiss MR; Daly KA; Ross JA; McCann M; Jurek AM; Berry SA Genet Med; 2011 Dec; 13(12):1006-10. PubMed ID: 21912263 [TBL] [Abstract][Full Text] [Related]
23. GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China. Shi GZ; Gong LX; Xu XH; Nie WY; Lin Q; Qi YS Hear Res; 2004 Nov; 197(1-2):19-23. PubMed ID: 15504600 [TBL] [Abstract][Full Text] [Related]
24. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China. Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. Gene Screening for Non-Syndromic Deafness in Hainanese Patients. Fu Y; Zhao Z; Zheng J; Zhu Y; Sun L J Int Adv Otol; 2023 Jul; 19(4):283-287. PubMed ID: 37528592 [TBL] [Abstract][Full Text] [Related]
27. [The effects of newborn genetic screening for GJB2 and hearing follow-ups]. Gao R; Chen X; Li D; Jiang H Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Feb; 29(4):314-8. PubMed ID: 26121828 [TBL] [Abstract][Full Text] [Related]
28. Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array. He X; Li X; Guo Y; Zhao Y; Dong H; Dong J; Zhong L; Shi Z; Zhang Y; Soliman M; Song C; Zhao Z Am J Audiol; 2018 Mar; 27(1):57-66. PubMed ID: 29234782 [TBL] [Abstract][Full Text] [Related]
29. Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population. Han SH; Park HJ; Kang EJ; Ryu JS; Lee A; Yang YH; Lee KR J Hum Genet; 2008; 53(11-12):1022-1028. PubMed ID: 19043807 [TBL] [Abstract][Full Text] [Related]
30. GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population. Yen TT; Chen IC; Cho S; Chang TG; Shih KH; Hua MW; Li JL; Hsu CY; Hsiao TH; Chen YM Ear Hear; 2023 Nov-Dec 01; 44(6):1423-1429. PubMed ID: 37271870 [TBL] [Abstract][Full Text] [Related]
31. Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program. Ruan Y; Wen C; Cheng X; Zhang W; Zhao L; Xie J; Lu H; Ren Y; Meng F; Li Y; Deng L; Huang L; Han D Biosci Trends; 2024 Sep; 18(4):303-314. PubMed ID: 39183030 [TBL] [Abstract][Full Text] [Related]
32. Newborn dried blood-spot screening of the p.V37I variant of GJB2 by high-resolution melting analysis. Chen Y; Li L; Sun LH; Yang T; Wu H Int J Pediatr Otorhinolaryngol; 2014 Jul; 78(7):1080-3. PubMed ID: 24814571 [TBL] [Abstract][Full Text] [Related]
33. [Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]. Wang G; Yuan Y; Li R; Han M; Huang S; Kang D; Zhang X; Dong M; Dai P; Han D Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 May; 25(10):445-8. PubMed ID: 21809555 [TBL] [Abstract][Full Text] [Related]
34. GJB2 mutations and degree of hearing loss: a multicenter study. Snoeckx RL; Huygen PL; Feldmann D; Marlin S; Denoyelle F; Waligora J; Mueller-Malesinska M; Pollak A; Ploski R; Murgia A; Orzan E; Castorina P; Ambrosetti U; Nowakowska-Szyrwinska E; Bal J; Wiszniewski W; Janecke AR; Nekahm-Heis D; Seeman P; Bendova O; Kenna MA; Frangulov A; Rehm HL; Tekin M; Incesulu A; Dahl HH; du Sart D; Jenkins L; Lucas D; Bitner-Glindzicz M; Avraham KB; Brownstein Z; del Castillo I; Moreno F; Blin N; Pfister M; Sziklai I; Toth T; Kelley PM; Cohn ES; Van Maldergem L; Hilbert P; Roux AF; Mondain M; Hoefsloot LH; Cremers CW; Löppönen T; Löppönen H; Parving A; Gronskov K; Schrijver I; Roberson J; Gualandi F; Martini A; Lina-Granade G; Pallares-Ruiz N; Correia C; Fialho G; Cryns K; Hilgert N; Van de Heyning P; Nishimura CJ; Smith RJ; Van Camp G Am J Hum Genet; 2005 Dec; 77(6):945-57. PubMed ID: 16380907 [TBL] [Abstract][Full Text] [Related]
35. [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]
37. Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow-up. Kun L; Jiexiang H; Hua L; Junlin H; Yijun R; Lixian Z; Mingqiao C Mol Genet Genomic Med; 2024 Jan; 12(1):e2324. PubMed ID: 38037722 [TBL] [Abstract][Full Text] [Related]
38. Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns. Oguchi T; Ohtsuka A; Hashimoto S; Oshima A; Abe S; Kobayashi Y; Nagai K; Matsunaga T; Iwasaki S; Nakagawa T; Usami SI J Hum Genet; 2005; 50(2):76-83. PubMed ID: 15700112 [TBL] [Abstract][Full Text] [Related]
39. [Analysis of genotypes and audiological characteristics of children with SLC26A4 gene pathogenic mutations]. Zhao XL; Huang LH; Wang XY; DU Y; Wang X; Cheng XH; Zhao LP; Li Y Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):836-840. PubMed ID: 29921053 [No Abstract] [Full Text] [Related]
40. [Analysis of mutations of 4 common genes among 216 patients with non-syndromic hearing impairment]. Li C; Lu D; Chen X; Huang B; Chen K; Liu X; Hu A; Zhang Y; Xue X; Xing Y; Yan Z; Dong X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):630-633. PubMed ID: 30298483 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]