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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

106 related items for PubMed ID: 10590915

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  • 3. Deafness genes.
    Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H.
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
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  • 4. Nonsyndromic hearing loss.
    Van Laer L, Cryns K, Smith RJ, Van Camp G.
    Ear Hear; 2003 Aug; 24(4):275-88. PubMed ID: 12923419
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  • 6. [Hereditary hearing loss: new diagnostic possibilities].
    Hergersberg M, Weigell-Weber M.
    Schweiz Med Wochenschr; 2000 Apr 01; 130(13):485-9. PubMed ID: 10812644
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  • 7. Novel TECTA mutations identified in stable sensorineural hearing loss and their clinical implications.
    Kim AR, Chang MY, Koo JW, Oh SH, Choi BY.
    Audiol Neurootol; 2015 Apr 01; 20(1):17-25. PubMed ID: 25413827
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  • 8. A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9.
    Masuda M, Mutai H, Arimoto Y, Nakano A, Matsunaga T.
    Biochem Biophys Res Commun; 2016 Jan 08; 469(2):270-4. PubMed ID: 26631968
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  • 11. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.
    Mesolella M, Tranchino G, Nardone M, Motta S, Galli V.
    Int J Pediatr Otorhinolaryngol; 2004 Aug 08; 68(8):995-1005. PubMed ID: 15236885
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  • 12. [Genetic study of sensorineural hearing loss].
    Bliumina MG, Moskovkina AG.
    Genetika; 1982 Aug 08; 18(6):1012-7. PubMed ID: 7201942
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  • 15. A stepwise approach to the diagnosis and treatment of hereditary hearing loss.
    Tomaski SM, Grundfast KM.
    Pediatr Clin North Am; 1999 Feb 08; 46(1):35-48. PubMed ID: 10079788
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  • 16. The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report.
    Nam GS, Rim JH, Choi JY, Gee HY, Choi JR, Lee ST, Jung J.
    BMC Med Genet; 2019 Apr 01; 20(1):57. PubMed ID: 30935366
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  • 17. Nonsyndromic hereditary hearing loss.
    Li XC, Friedman RA.
    Otolaryngol Clin North Am; 2002 Apr 01; 35(2):275-85. PubMed ID: 12391618
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