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Journal Abstract Search

101 related items for PubMed ID: 1952625

  • 1. Similarities between mice and humans with hereditary deafness.
    Steel KP.
    Ann N Y Acad Sci; 1991; 630():68-79. PubMed ID: 1952625
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  • 2. Unconventional myosins, the basis for deafness in mouse and man.
    Hasson T.
    Am J Hum Genet; 1997 Oct; 61(4):801-5. PubMed ID: 9382088
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  • 5. Reverse genetic approaches to cloning deafness genes.
    Brown SD, Brown KA, Sutcliffe MJ, Cavanna JS, Greenfield AJ, Steel KP.
    Ann N Y Acad Sci; 1991 Oct; 630():93-9. PubMed ID: 1952627
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  • 10. Targeted disruption of otog results in deafness and severe imbalance.
    Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ.
    Nat Genet; 2000 Feb; 24(2):139-43. PubMed ID: 10655058
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  • 12. [Hereditary nephritis with inner ear deafness (Alport syndrome)].
    Lachhein L, Kemnitz P, Büttner H, Thal W, Witkowski R.
    Dtsch Med Wochenschr; 1968 Oct 04; 93(40):1891-6. PubMed ID: 5679121
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  • 13. Genes responsible for human hereditary deafness: symphony of a thousand.
    Petit C.
    Nat Genet; 1996 Dec 04; 14(4):385-91. PubMed ID: 8944017
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  • 16. Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein.
    Ikezono T, Omori A, Ichinose S, Pawankar R, Watanabe A, Yagi T.
    Biochim Biophys Acta; 2001 Mar 26; 1535(3):258-65. PubMed ID: 11278165
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  • 18. [Hereditary associated morphodysplasia of ear and eye].
    Morgon A, Pauper-Ravault M, Haguenauer JP.
    J Fr Otorhinolaryngol Chir Maxillofac; 1966 Sep 26; 15(5):597-608. PubMed ID: 4959666
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  • 19. [Alport's syndrome and associated congenital malformations of the kidney and ear].
    Bérard F, Morand R.
    Ann Otolaryngol Chir Cervicofac; 1967 Sep 26; 84(7):555-60. PubMed ID: 6073014
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  • 20. Genetic deafness of central origin.
    Deol MS, Frank MP, Steel KP, Bock GR.
    Brain Res; 1983 Jan 03; 258(1):177-9. PubMed ID: 24010186
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