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Pubmed for Handhelds

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Journal Abstract Search

119 related items for PubMed ID: 10889003

  • 21. Isolated large vestibular aqueduct syndrome in a family.
    Nowak KC, Messner AH.
    Ann Otol Rhinol Laryngol; 2000 Jan; 109(1):40-4. PubMed ID: 10651410
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  • 26. Phenotype description of a novel DFNA9/COCH mutation, I109T.
    Pauw RJ, Huygen PL, Collin RW, Cruysberg JR, Hoefsloot LH, Kremer H, Cremers CW.
    Ann Otol Rhinol Laryngol; 2007 May; 116(5):349-57. PubMed ID: 17561763
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  • 29. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
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  • 30. Audio-vestibular disturbances in Behcet's patients: report of 62 cases.
    Kulahli I, Balci K, Koseoglu E, Yuce I, Cagli S, Senturk M.
    Hear Res; 2005 May; 203(1-2):28-31. PubMed ID: 15855027
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  • 31. Large vestibular aqueduct syndrome: audiological, radiological, clinical, and genetic features.
    Berrettini S, Forli F, Bogazzi F, Neri E, Salvatori L, Casani AP, Franceschini SS.
    Am J Otolaryngol; 2005 May; 26(6):363-71. PubMed ID: 16275403
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  • 35. Audiologic and vestibular findings in a sample of human immunodeficiency virus type-1-infected Mexican children under highly active antiretroviral therapy.
    Palacios GC, Montalvo MS, Fraire MI, Leon E, Alvarez MT, Solorzano F.
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1671-81. PubMed ID: 18814921
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  • 37. Audiological and radiological characteristics of a family with T961G mitochondrial mutation.
    Turchetta R, Mazzei F, Celani T, Cammeresi MG, Orlando MP, Altissimi G, de Vincentiis C, D'Ambrosio F, Messineo D, Ferraris A, Cianfrone G.
    Int J Audiol; 2012 Dec; 51(12):870-9. PubMed ID: 23013294
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  • 39. Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus.
    Rad A, Schade-Mann T, Gamerdinger P, Yanus GA, Schulte B, Müller M, Imyanitov EN, Biskup S, Löwenheim H, Tropitzsch A, Vona B.
    Hum Mutat; 2021 Jan; 42(1):25-30. PubMed ID: 33169910
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  • 40. Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice.
    Szymko-Bennett YM, Kurima K, Olsen B, Seegmiller R, Griffith AJ.
    Hear Res; 2003 Jan; 175(1-2):178-82. PubMed ID: 12527136
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