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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

198 related items for PubMed ID: 11449319

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  • 5. Phenotype in two families with RP3 associated with RPGR mutations.
    Lorenz B, Andrassi M, Kretschmann U.
    Ophthalmic Genet; 2003 Jun; 24(2):89-101. PubMed ID: 12789573
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  • 8. Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1.
    Dessalces E, Bocquet B, Bourien J, Zanlonghi X, Verdet R, Meunier I, Hamel CP.
    JAMA Ophthalmol; 2013 Oct; 131(10):1314-23. PubMed ID: 23929416
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  • 10. A homozygous frameshift mutation in LRAT causes retinitis punctata albescens.
    Littink KW, van Genderen MM, van Schooneveld MJ, Visser L, Riemslag FC, Keunen JE, Bakker B, Zonneveld MN, den Hollander AI, Cremers FP, van den Born LI.
    Ophthalmology; 2012 Sep; 119(9):1899-906. PubMed ID: 22559933
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  • 14. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan; 30(1):51-62. PubMed ID: 19952985
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  • 15. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
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  • 19. Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy.
    Mäntyjärvi M, Nurmenniemi P, Partanen J, Myöhänen T, Peippo M, Alitalo T.
    Acta Ophthalmol Scand; 2001 Aug; 79(4):359-65. PubMed ID: 11453854
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