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Journal Abstract Search

1085 related items for PubMed ID: 15603707

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
    Liu XZ, Xia XJ, Ke XM, Ouyang XM, Du LL, Liu YH, Angeli S, Telischi FF, Nance WE, Balkany T, Xu LR.
    Hum Genet; 2002 Oct; 111(4-5):394-7. PubMed ID: 12384781
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.
    Liu Y, Ke X, Qi Y, Li W, Zhu P.
    J Hum Genet; 2002 Jun 16; 47(12):688-90. PubMed ID: 12522692
    [Abstract] [Full Text] [Related]

  • 5. Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.
    Gazzaz B, Weil D, Raïs L, Akhyat O, Azeddoug H, Nadifi S.
    Hear Res; 2005 Dec 16; 210(1-2):80-4. PubMed ID: 16243461
    [Abstract] [Full Text] [Related]

  • 6. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
    Davarnia B, Babanejad M, Fattahi Z, Nikzat N, Bazazzadegan N, Pirzade A, Farajollahi R, Nishimura C, Jalalvand K, Arzhangi S, Kahrizi K, Smith RJ, Najmabadi H.
    Int J Pediatr Otorhinolaryngol; 2012 Feb 16; 76(2):268-71. PubMed ID: 22172221
    [Abstract] [Full Text] [Related]

  • 7. Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan.
    Wang YC, Kung CY, Su MC, Su CC, Hsu HM, Tsai CC, Lin CC, Li SY.
    Eur J Hum Genet; 2002 Aug 16; 10(8):495-8. PubMed ID: 12111646
    [Abstract] [Full Text] [Related]

  • 8. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.
    Rabionet R, Zelante L, López-Bigas N, D'Agruma L, Melchionda S, Restagno G, Arbonés ML, Gasparini P, Estivill X.
    Hum Genet; 2000 Jan 16; 106(1):40-4. PubMed ID: 10982180
    [Abstract] [Full Text] [Related]

  • 9. Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population.
    Al-Janabi AM, Ahmmed HS, Al-Khafaji SM.
    J Med Life; 2021 Jan 16; 14(6):841-846. PubMed ID: 35126756
    [Abstract] [Full Text] [Related]

  • 10. 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 16; 197(1-2):19-23. PubMed ID: 15504600
    [Abstract] [Full Text] [Related]

  • 11. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M, Bahri W, Habibi M, Zainine R, Maazoul F, Ghazi B, Chaabouni H, Mrad R.
    Int J Pediatr Otorhinolaryngol; 2013 May 16; 77(5):714-6. PubMed ID: 23434199
    [Abstract] [Full Text] [Related]

  • 12. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A, Al Mutery A, Kamal Eddine Ahmad Mohamed W, Mahfood M, Hadj Kacem H.
    Genet Test Mol Biomarkers; 2017 Nov 16; 21(11):686-691. PubMed ID: 29016196
    [Abstract] [Full Text] [Related]

  • 13. [GJB2 gene mutation in deaf patients].
    Xu ZY, Gao GF, Liu C, Hu YH, Lin Y, Zhang RZ, Liu M, Wang SY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr 16; 26(2):144-6. PubMed ID: 19350503
    [Abstract] [Full Text] [Related]

  • 14. 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 16; 10(1):379-86. PubMed ID: 24737404
    [Abstract] [Full Text] [Related]

  • 15. Connexin-26 mutations in sporadic and inherited sensorineural deafness.
    Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield E, Rappaport E, Govea N, Milà M, Zelante L, Gasparini P.
    Lancet; 1998 Feb 07; 351(9100):394-8. PubMed ID: 9482292
    [Abstract] [Full Text] [Related]

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  • 17. Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
    Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB.
    Int J Pediatr Otorhinolaryngol; 2002 Sep 02; 65(2):101-8. PubMed ID: 12176179
    [Abstract] [Full Text] [Related]

  • 18. Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.
    Cordeiro-Silva Mde F, Barbosa A, Santiago M, Provetti M, Dettogni RS, Tovar TT, Rabbi-Bortolini E, Louro ID.
    Mol Biol Rep; 2011 Feb 02; 38(2):1309-13. PubMed ID: 20563649
    [Abstract] [Full Text] [Related]

  • 19. 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 02; 30(1):1-7. PubMed ID: 19125024
    [Abstract] [Full Text] [Related]

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