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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

84 related items for PubMed ID: 646734

  • 21. Superior ultra-audiometric hearing associated with genetic hearing loss.
    Bergstrom L, Morgan D.
    Otolaryngol Head Neck Surg; 1983 Feb; 91(1):33-40. PubMed ID: 6405347
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  • 23. [Non-syndromic familial deafness. Review and genetic study].
    Guiral H, Flores JC, Risco J, Figuerola E, Pellicer F.
    Acta Otorrinolaringol Esp; 1996 Feb; 47(4):272-6. PubMed ID: 8962727
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  • 25. Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.
    Topsakal V, Hilgert N, van Dinther J, Tranebjaerg L, Rendtorff ND, Zarowski A, Offeciers E, Van Camp G, van de Heyning P.
    Audiol Neurootol; 2010 Feb; 15(4):211-20. PubMed ID: 19893302
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  • 31. Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3.
    van Beelen E, Schraders M, Huygen PL, Oostrik J, Plantinga RF, van Drunen W, Collin RW, Kooper DP, Pennings RJ, Cremers CW, Kremer H, Kunst HP.
    Hear Res; 2013 Jun; 300():10-7. PubMed ID: 23538131
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  • 36. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].
    Jin Z, Cheng J, Lu Y, Li J, Sun Y, Yuan H, Han D.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462
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  • 37. [Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss].
    Graf K.
    Laryngorhinootologie; 1992 May; 71(5):242-5. PubMed ID: 1616543
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