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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 24506996)

  • 1. [Application of MALDI-TOF-MS in gene testing for non-syndromic hearing loss].
    Zeng Y; Jiang D; Feng DF; Jin DD; Wu XH; Ding YL; Zou J
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Dec; 48(12):985-90. PubMed ID: 24506996
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [An analysis of the mutation in GJB2,GJB3,SLC26A4 and mtDNA12SrRNA in new born].
    Chai F; Zhao HL; Qiu SQ
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 May; 31(9):664-666. PubMed ID: 29871341
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [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]  

  • 6. [Mutation spectrum analysis of 23-site chip neonatal deafness genetic screening].
    Ruan Y; Cheng X; Zhang W; Zhao L; Xie J; Wen C; Li Y; Deng L; Huang L
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Apr; 38(4):267-272. PubMed ID: 38563166
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum.
    Chen K; Zong L; Liu M; Wang X; Zhou W; Zhan Y; Cao H; Dong C; Tang H; Jiang H
    J Transl Med; 2014 Mar; 12():64. PubMed ID: 24612839
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. [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]  

  • 11. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
    Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
    Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. [Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].
    Wang YL; Zhu YM; Liu XW; Xu BC; Guo YF; Wang QJ
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 47(9):760-3. PubMed ID: 23141447
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
    Chen T; Liu Q; Jiang L; Liu C; Ou Q
    Genet Test Mol Biomarkers; 2013 Feb; 17(2):122-30. PubMed ID: 23256547
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.
    Ma Y; Xiao Y; Bai X; Zhang F; Zhang D; Xu X; Xu L; Wang H
    Acta Otolaryngol; 2016 Aug; 136(8):800-5. PubMed ID: 27066914
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Detection of common deafness-related genes among non-syndromic deafness patients from Shanxi province].
    Zhou Y; Yang H; Hao Z; Ma Y; Zhang Q; Li J; Zhao X; Wang X; Li X; Xia L; Ma S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):183-6. PubMed ID: 25863082
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.