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Journal Abstract Search

147 related items for PubMed ID: 8741120

  • 21. Tractional retinal detachment in Usher syndrome type II.
    Rani A, Pal N, Azad RV, Sharma YR, Chandra P, Vikram Singh D.
    Clin Exp Ophthalmol; 2005 Aug; 33(4):436-7. PubMed ID: 16033369
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  • 22. [The incidence of Usher's syndrome and its clinical types].
    Bereketoğlu M, Avşar EU, Turan O, Afrashi F, Apaydin F.
    Kulak Burun Bogaz Ihtis Derg; 2002 Aug; 9(1):15-20. PubMed ID: 12122620
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  • 28. Vestibular and auditory function in Usher's syndrome.
    Kumar A, Fishman G, Torok N.
    Ann Otol Rhinol Laryngol; 1984 Aug; 93(6 Pt 1):600-8. PubMed ID: 6334472
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  • 29. Fuchs' heterochromic cyclitis associated with retinitis pigmentosa: a family study.
    Vuorre I, Saari M, Tiilikainen A, Rasanen O.
    Can J Ophthalmol; 1979 Jan; 14(1):10-6. PubMed ID: 421158
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  • 32. Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
    Aller E, Jaijo T, Oltra S, Alió J, Galán F, Nájera C, Beneyto M, Millán JM.
    Clin Genet; 2004 Dec; 66(6):525-9. PubMed ID: 15521980
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  • 33. Clinical presentation of DFNB12 and Usher syndrome type 1D.
    Bork JM, Morell RJ, Khan S, Riazuddin S, Wilcox ER, Friedman TB, Griffith AJ.
    Adv Otorhinolaryngol; 2002 Dec; 61():145-52. PubMed ID: 12408077
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  • 36. Retinitis pigmentosa, hearing loss and vitiligo: report of two patients.
    Dereymaeker AM, Fryns JP, Ars J, Andresescu J, van den Berghe H.
    Clin Genet; 1989 May; 35(5):387-9. PubMed ID: 2758690
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  • 37. Exome sequencing extends the phenotypic spectrum for ABHD12 mutations: from syndromic to nonsyndromic retinal degeneration.
    Nishiguchi KM, Avila-Fernandez A, van Huet RA, Corton M, Pérez-Carro R, Martín-Garrido E, López-Molina MI, Blanco-Kelly F, Hoefsloot LH, van Zelst-Stams WA, García-Ruiz PJ, Del Val J, Di Gioia SA, Klevering BJ, van de Warrenburg BP, Vazquez C, Cremers FP, García-Sandoval B, Hoyng CB, Collin RW, Rivolta C, Ayuso C.
    Ophthalmology; 2014 Aug; 121(8):1620-7. PubMed ID: 24697911
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  • 38. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
    Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D.
    Hum Genet; 2002 Apr; 110(4):348-50. PubMed ID: 11941484
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  • 40. [Hypacusis in retinitis pigmentosa].
    Martini A, Magnan G, Steindler P, Tormene AP, Molinari G.
    Acta Otorhinolaryngol Ital; 1983 Apr; 3(1):63-9. PubMed ID: 6880704
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