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Journal Abstract Search

187 related items for PubMed ID: 7711740

  • 1. Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
    Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A.
    Hum Mol Genet; 1995 Jan; 4(1):93-8. PubMed ID: 7711740
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  • 2. Further refinement of the Usher 2A locus at 1q41.
    Bessant DA, Payne AM, Plant C, Bird AC, Bhattacharya SS.
    J Med Genet; 1998 Sep; 35(9):773-4. PubMed ID: 9733039
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  • 8. [Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].
    Espinós C, Pérez-Garrigues H, Beneyto M, Vilela C, Rodrigo O, Nájera C.
    An Otorrinolaringol Ibero Am; 1999 Sep; 26(1):83-95. PubMed ID: 10091368
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  • 9. Identification of a novel locus for a USH3 like syndrome combined with congenital cataract.
    Dad S, Østergaard E, Thykjaer T, Albrectsen A, Ravn K, Rosenberg T, Møller LB.
    Clin Genet; 2010 Oct; 78(4):388-97. PubMed ID: 20236115
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  • 16. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, Millán JM, Aller E, Mitter D, Bolz H.
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
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  • 17. Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.
    Pieke-Dahl S, Möller CG, Kelley PM, Astuto LM, Cremers CW, Gorin MB, Kimberling WJ.
    J Med Genet; 2000 Apr; 37(4):256-62. PubMed ID: 10745043
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  • 18. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2).
    Beneyto MM, Cuevas JM, Millán JM, Espinós C, Mateu E, González-Cabo P, Baiget M, Doménech M, Bernal S, Ayuso C, García-Sandoval B, Trujillo MJ, Borrego S, Antiñolo G, Carballo M, Nájera C.
    Ophthalmic Genet; 2000 Jun; 21(2):123-8. PubMed ID: 10916187
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