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Journal Abstract Search

187 related items for PubMed ID: 9600457

  • 1.
    ; . PubMed ID:
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  • 2. Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss.
    Erbe CB, Harris KC, Runge-Samuelson CL, Flanary VA, Wackym PA.
    Laryngoscope; 2004 Apr; 114(4):607-11. PubMed ID: 15064611
    [Abstract] [Full Text] [Related]

  • 3. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.
    del Castillo I, Villamar M, Moreno-Pelayo MA, del Castillo FJ, Alvarez A, Tellería D, Menéndez I, Moreno F.
    N Engl J Med; 2002 Jan 24; 346(4):243-9. PubMed ID: 11807148
    [Abstract] [Full Text] [Related]

  • 4. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
    Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ.
    Am J Hum Genet; 1998 Apr 24; 62(4):792-9. PubMed ID: 9529365
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  • 5. 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 24; 76(2):268-71. PubMed ID: 22172221
    [Abstract] [Full Text] [Related]

  • 6. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).
    Lench NJ, Markham AF, Mueller RF, Kelsell DP, Smith RJ, Willems PJ, Schatteman I, Capon H, Van De Heyning PJ, Van Camp G.
    J Med Genet; 1998 Feb 24; 35(2):151-2. PubMed ID: 9507396
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12.
    Kelley PM, Abe S, Askew JW, Smith SD, Usami Si, Kimberling WJ.
    Genomics; 1999 Dec 01; 62(2):172-6. PubMed ID: 10610709
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 117(12):1797-801. PubMed ID: 15603707
    [Abstract] [Full Text] [Related]

  • 10. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).
    Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, Schaefer GB, Gobar LS, Hahn FJ, Harris DJ, Kimberling WJ.
    Pediatrics; 1999 Mar 01; 103(3):546-50. PubMed ID: 10049954
    [Abstract] [Full Text] [Related]

  • 11. Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.
    Meyer NC, Alasti F, Nishimura CJ, Imanirad P, Kahrizi K, Riazalhosseini Y, Malekpour M, Kochakian N, Jamali P, Van Camp G, Smith RJ, Najmabadi H.
    Am J Med Genet A; 2007 Jul 15; 143A(14):1623-9. PubMed ID: 17431902
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 210(1-2):80-4. PubMed ID: 16243461
    [Abstract] [Full Text] [Related]

  • 13.
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  • 14. A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.
    Leshinsky-Silver E, Berman Z, Vinkler C, Yannov-Sharav M, Lev D.
    Hear Res; 2005 Apr 15; 202(1-2):258-61. PubMed ID: 15811717
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  • 15.
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  • 16. A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness.
    Frei K, Lucas T, Ramsebner R, Schöfer C, Baumgartner WD, Weipoltshammer K, Erginel-Unaltuna N, Wachtler FJ, Kirschhofer K.
    Audiol Neurootol; 2004 Apr 15; 9(1):47-50. PubMed ID: 14676473
    [Abstract] [Full Text] [Related]

  • 17. [Mutations in the connexin 26 gene in patients with nonsyndromic hearing impairment].
    Xiao Z, Feng Y, Pan Q, Xie D, Shi X, Xia J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Jun 15; 35(3):188-91. PubMed ID: 12768774
    [Abstract] [Full Text] [Related]

  • 18. Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.
    Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, Morell RJ, Friedman TB.
    Am J Hum Genet; 2000 Sep 15; 67(3):745-9. PubMed ID: 10903123
    [Abstract] [Full Text] [Related]

  • 19. Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
    Hashemi SB, Ashraf MJ, Saboori M, Azarpira N, Darai M.
    Mol Biol Rep; 2012 Dec 15; 39(12):10481-7. PubMed ID: 23073770
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