BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 29605365)

  • 21. 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]  

  • 22. [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]  

  • 23. [Molecular etiology analysis among students with profound hearing loss in a special education school in Yangzhou].
    Peng X; Li X; Xu L; Guan B; Zhang J; Yu A
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Jul; 26(13):577-80. PubMed ID: 23002639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. 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]  

  • 26. Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.
    Du W; Wang Q; Zhu Y; Wang Y; Guo Y
    Biomed Res Int; 2014; 2014():746838. PubMed ID: 24804242
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Analysis of GJB2, SLC26A4, GJB3 and 12S rRNA gene mutations among patients with nonsyndromic hearing loss from eastern Shandong].
    Sun S; Niu L; Tian J; Chen W; Li Y; Xia N; Jyu C; Chen X; Zhang C; Lan X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):433-438. PubMed ID: 31030427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. [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]  

  • 31. Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study.
    Chen Y; Tudi M; Sun J; He C; Lu HL; Shang Q; Jiang D; Kuyaxi P; Hu B; Zhang H
    J Transl Med; 2011 Sep; 9():154. PubMed ID: 21917135
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].
    Ji YB; Han DY; Wang DY; Zhou Y; Zhao C; Wang H; Lan L; Wang QJ
    Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2531-5. PubMed ID: 20137612
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Deafness Gene Mutations in Newborns in the Foshan Area of South China With Bloodspot-Based Genetic Screening Tests.
    Cao S; Sha Y; Ke P; Li T; Yuan W; Huang X
    Am J Audiol; 2020 Jun; 29(2):165-169. PubMed ID: 32208970
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss.
    Yao G; Chen D; Wang H; Li S; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
    Acta Otolaryngol; 2013 Aug; 133(8):833-41. PubMed ID: 23638949
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
    Luo J; Bai X; Zhang F; Xiao Y; Gu L; Han Y; Fan Z; Li J; Xu L; Wang H
    Ann Hum Genet; 2017 Nov; 81(6):258-266. PubMed ID: 28786104
    [TBL] [Abstract][Full Text] [Related]  

  • 37. GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.
    Guo YF; Liu XW; Guan J; Han MK; Wang DY; Zhao YL; Rao SQ; Wang QJ
    Acta Otolaryngol; 2008 Mar; 128(3):297-303. PubMed ID: 18274916
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.