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 *

270 related articles for article (PubMed ID: 25999548)

  • 21. [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]  

  • 22. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
    Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Prevalence of mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 genes in 103 children with sensorineural hearing loss in Shaoxing, China.
    Yu H; Liu D; Yang J; Wu Z
    Ear Nose Throat J; 2018 Jun; 97(6):E33-E38. PubMed ID: 30036422
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
    Zhang F; Xiao Y; Xu L; Zhang X; Zhang G; Li J; Lv H; Bai X; Wang H
    Biomed Res Int; 2016; 2016():1302914. PubMed ID: 27247933
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [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]  

  • 28. Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation.
    Chen K; Wang X; Sun L; Jiang H
    Otolaryngol Head Neck Surg; 2012 Jun; 146(6):972-8. PubMed ID: 22412181
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography].
    Zhao J; Wu LQ; Feng Y; Pan Q; Zhao K; Li HY; Liang DS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):21-5. PubMed ID: 19199245
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Prenatal genetic counseling and instruction for deaf families by genetic test].
    Han MY; Huang SS; Wang GJ; Yuan YY; Kang DY; Zhang X; Dai P
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Nov; 46(11):909-13. PubMed ID: 22335977
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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]  

  • 32. [Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].
    Yang A; Geng M; Zhang H; Guo X; Tang J; Han F
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1959-62. PubMed ID: 26911058
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Newborn genetic screening for hearing impairment: a population-based longitudinal study.
    Wu CC; Tsai CH; Hung CC; Lin YH; Lin YH; Huang FL; Tsao PN; Su YN; Lee YL; Hsieh WS; Hsu CJ
    Genet Med; 2017 Jan; 19(1):6-12. PubMed ID: 27308839
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Analysis and prenatal diagnosis of deafness-related gene mutations in patients with nonsyndromic hearing loss].
    Li H; Chen Y; Mao Y; Ding Y; Xu X; Tang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):553-6. PubMed ID: 25297579
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Comparison of the Mutation Spectrum of Common Deafness-Causing Genes in 509 Patients With Nonsyndromic Hearing Loss in 4 Different Areas of China by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry.
    Wang Y; Chen W; Liu Z; Xing W; Zhang H
    J Int Adv Otol; 2021 Nov; 17(6):492-499. PubMed ID: 35177385
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. 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]  

  • 39. The effect of GJB2 and SLC26A4 gene mutations on rehabilitative outcomes in pediatric cochlear implant patients.
    Yan YJ; Li Y; Yang T; Huang Q; Wu H
    Eur Arch Otorhinolaryngol; 2013 Nov; 270(11):2865-70. PubMed ID: 23296490
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Genetic counseling and instruction for deaf couples directed by genetic testing].
    Han B; Dai P; Wang GJ; Kang DY; Zhang X; Yuan YY; Zhu QW; Jin ZC; Li M; Zhai SQ; Huang DL; Han DY
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Jul; 42(7):499-503. PubMed ID: 17886676
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.