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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

143 related items for PubMed ID: 8794099

  • 21.
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  • 23. Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse.
    Tian C, Liu XZ, Han F, Yu H, Longo-Guess C, Yang B, Lu C, Yan D, Zheng QY.
    Brain Res; 2010 Apr 30; 1328():57-70. PubMed ID: 20211154
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  • 26. Quantitative measures reflect degeneration, but not regeneration, in the deafness mouse organ of Corti.
    Faddis BT, Hughes RM, Miller JD.
    Hear Res; 1998 Jan 30; 115(1-2):6-12. PubMed ID: 9472731
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  • 30. [Histology of hereditary, recessive deaf-mutism].
    Secrétan JP, Neiger M.
    Acta Otolaryngol; 1970 Apr 30; 69(4):273-80. PubMed ID: 5445960
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  • 32. [The Waardenburg-Klein syndrome].
    ARNVIG J.
    Nord Med; 1960 Jul 28; 64():953-5. PubMed ID: 13794441
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  • 34. Development of the vertebrate ear: insights from knockouts and mutants.
    Fekete DM.
    Trends Neurosci; 1999 Jun 28; 22(6):263-9. PubMed ID: 10354604
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  • 35. An introduction to the genetics of normal and defective hearing.
    Martini A, Mazzoli M, Kimberling W.
    Ann N Y Acad Sci; 1997 Dec 29; 830():361-74. PubMed ID: 9616696
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  • 38. Inner ear pathology of congenital deafness.
    Beal DD, Davey PR, Lindsay JR.
    Arch Otolaryngol; 1967 Feb 29; 85(2):134-42. PubMed ID: 6017585
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  • 39. Tomography of the inner ear in a case of Waardenburg's syndrome.
    Jensen J.
    Am J Roentgenol Radium Ther Nucl Med; 1967 Dec 29; 101(4):828-33. PubMed ID: 6073377
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  • 40. Spontaneous mutant ICR kuru2 might be another shaker-2 deaf mouse.
    Watanabe M, Akiyama N, Manome Y, Hasegawa N.
    In Vivo; 2012 Dec 29; 26(5):787-91. PubMed ID: 22949591
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