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231 related items for PubMed ID: 15793769

  • 1. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
    Xu C, Zhang H, Zhang Y, Zhao S, Geng X, Shan Y, Shan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):125-8. PubMed ID: 15793769
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  • 2. [GJB2 235delC single allelic mutation modulates the phenotype associated with the mitochondrial A1555G mutation].
    Li Q, Fang RP, Zhou HG, Dai P, Tian L, Lin D, Huang Q, Song JM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):194-7. PubMed ID: 20376804
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  • 3. [Sequence analysis of the connexin 26 genes from a deafness family with A1555G mutation in Huaiyin].
    Zhang HJ, Xu CH, Zhang YJ, Zhao SY, Geng XX, Shan YF, Fan G, Xing GQ, Shan XN, Bu XK.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2005 Sep; 40(9):678-83. PubMed ID: 16335400
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  • 4. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
    Gallo-Terán J, Morales-Angulo C, del Castillo I, Villamar M, Moreno-Pelayo MA, García-Mantilla J, Moreno F.
    Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
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  • 10. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA, Xie DH.
    Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
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  • 12. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
    Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ.
    Acta Otolaryngol; 2011 Feb; 131(2):124-9. PubMed ID: 21162657
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  • 13. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
    Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ.
    JAMA; 1999 Jun 16; 281(23):2211-6. PubMed ID: 10376574
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  • 14. GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.
    Baysal E, Bayazit YA, Ceylaner S, Alatas N, Donmez B, Ceylaner G, San I, Korkmaz B, Yilmaz A, Menevse A, Altunyay S, Gunduz B, Goksu N, Arslan A, Ekmekci A.
    J Genet; 2008 Apr 16; 87(1):53-7. PubMed ID: 18560174
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  • 15. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
    Birkenhäger R, Zimmer AJ, Maier W, Schipper J.
    Laryngorhinootologie; 2006 Mar 16; 85(3):191-6. PubMed ID: 16547895
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  • 17. Cx26 gene mutations in idiopathic progressive hearing loss.
    Ravecca F, Berrettini S, Forli F, Marcaccini M, Casani A, Baldinotti F, Fogli A, Siciliano G, Simi P.
    J Otolaryngol; 2005 Apr 16; 34(2):126-34. PubMed ID: 16076412
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