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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 14676473

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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; 76(2):268-71. PubMed ID: 22172221
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.
    Janecke AR, Nekahm D, Löffler J, Hirst-Stadlmann A, Müller T, Utermann G.
    Hum Genet; 2001 Mar 16; 108(3):269-70. PubMed ID: 11354642
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.
    Richard G, Brown N, Ishida-Yamamoto A, Krol A.
    J Invest Dermatol; 2004 Nov 16; 123(5):856-63. PubMed ID: 15482471
    [Abstract] [Full Text] [Related]

  • 13. [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 16; 40(9):678-83. PubMed ID: 16335400
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [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 16; 53(8):563-71. PubMed ID: 12530196
    [Abstract] [Full Text] [Related]

  • 19. Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
    Löffler J, Nekahm D, Hirst-Stadlmann A, Günther B, Menzel HJ, Utermann G, Janecke AR.
    Eur J Hum Genet; 2001 Mar 16; 9(3):226-30. PubMed ID: 11313763
    [Abstract] [Full Text] [Related]

  • 20. Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.
    Frei K, Ramsebner R, Hamader G, Lucas T, Schoefer C, Baumgartner WD, Wachtler FJ, Kirschhofer K.
    Hear Res; 2004 Aug 16; 194(1-2):81-6. PubMed ID: 15276679
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.