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Journal Abstract Search

126 related items for PubMed ID: 16428895

  • 1. An overview of hereditary hearing loss.
    Bayazit YA, Yilmaz M.
    ORL J Otorhinolaryngol Relat Spec; 2006; 68(2):57-63. PubMed ID: 16428895
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  • 2. Genes and syndromic hearing loss.
    Keats BJ.
    J Commun Disord; 2002; 35(4):355-66. PubMed ID: 12160354
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  • 5. [Hereditary hearing loss].
    Tropitzsch A, Schade-Mann T, Gamerdinger P.
    HNO; 2023 Feb; 71(2):131-142. PubMed ID: 36526931
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  • 6. [Hereditary hearing loss: genetic counselling].
    Cabanillas Farpón R, Cadiñanos Bañales J.
    Acta Otorrinolaringol Esp; 2012 Feb; 63(3):218-29. PubMed ID: 21514544
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  • 7. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.
    Kumar S, Marres HA, Cremers CW, Kimberling WJ.
    Am J Med Genet; 1998 Apr 13; 76(5):395-401. PubMed ID: 9556298
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  • 8. Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome.
    Wu CC, Lu YC, Chen PJ, Yeh PL, Su YN, Hwu WL, Hsu CJ.
    Audiol Neurootol; 2010 Apr 13; 15(1):57-66. PubMed ID: 19648736
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  • 9. Sex-linked deafness.
    Petersen MB, Wang Q, Willems PJ.
    Clin Genet; 2008 Jan 13; 73(1):14-23. PubMed ID: 18005182
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  • 10. Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss.
    Lenarduzzi S, Morgan A, Faletra F, Cappellani S, Morgutti M, Mezzavilla M, Peruzzi A, Ghiselli S, Ambrosetti U, Graziano C, Seri M, Gasparini P, Girotto G.
    Hear Res; 2019 Sep 15; 381():107769. PubMed ID: 31387071
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  • 12. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
    Farah WI, Aminuddin BS, Ruszymah BH.
    Malays J Pathol; 2006 Jun 15; 28(1):23-33. PubMed ID: 17694956
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  • 13. Hereditary hearing loss: from human mutation to mechanism.
    Lenz DR, Avraham KB.
    Hear Res; 2011 Nov 15; 281(1-2):3-10. PubMed ID: 21664957
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  • 14. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W, Trembath R.
    Nat Genet; 1996 Apr 15; 12(4):421-3. PubMed ID: 8630497
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  • 15. Genotype phenotype correlations for hearing impairment: approaches to management.
    Hoefsloot LH, Feenstra I, Kunst HP, Kremer H.
    Clin Genet; 2014 Jun 15; 85(6):514-23. PubMed ID: 24547994
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  • 18. [Correlation between degree of mitochondrial DNA 1555 mutation and clinical phenotype of nonsyndromic hearing loss].
    Cheng ZJ, Zhang R, Yang B, Liu QC, Jiang L, Chen J, Chen Y, Ou QS.
    Zhonghua Yi Xue Za Zhi; 2009 Sep 29; 89(36):2536-9. PubMed ID: 20137613
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