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Journal Abstract Search

177 related items for PubMed ID: 21514544

  • 1. [Hereditary hearing loss: genetic counselling].
    Cabanillas Farpón R, Cadiñanos Bañales J.
    Acta Otorrinolaringol Esp; 2012; 63(3):218-29. PubMed ID: 21514544
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  • 2. [Genetic study of sensorineural hearing loss].
    Bliumina MG, Moskovkina AG.
    Genetika; 1982; 18(6):1012-7. PubMed ID: 7201942
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  • 4. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
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  • 6. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
    Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N.
    Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280
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  • 8. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS, Brown DJ, McMillan PM, Barker SE, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
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  • 9. [Progress in genetic testing and prevention of hereditary hearing disorders].
    Markova TG, Poliakov AV.
    Vestn Otorinolaringol; 2007 Aug; (4):7-10. PubMed ID: 17828104
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  • 10. [Unilateral hearing loss in childhood. An empirical analysis comparing bilateral hearing loss].
    Kiese-Himmel C, Kruse E.
    Laryngorhinootologie; 2001 Jan; 80(1):18-22. PubMed ID: 11272242
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  • 11. 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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  • 13. Genetic testing for hearing loss: different motivations for the same outcome.
    Dagan O, Hochner H, Levi H, Raas-Rothschild A, Sagi M.
    Am J Med Genet; 2002 Nov 22; 113(2):137-43. PubMed ID: 12407703
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  • 18. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.
    Akita J, Abe S, Shinkawa H, Kimberling WJ, Usami S.
    J Hum Genet; 2001 Nov 22; 46(7):355-61. PubMed ID: 11450843
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  • 19. Genetic testing for hearing impairment.
    Topsakal V, Van Camp G, Van de Heyning P.
    B-ENT; 2005 Nov 22; 1(3):125-35. PubMed ID: 16255497
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  • 20. Advances in genetic diagnostics for hereditary hearing loss.
    Idan N, Brownstein Z, Shivatzki S, Avraham KB.
    J Basic Clin Physiol Pharmacol; 2013 Nov 22; 24(3):165-70. PubMed ID: 24006325
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