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Pubmed for Handhelds

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Journal Abstract Search

378 related items for PubMed ID: 7591627

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  • 6. Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.
    Mizrahi-Meissonnier L, Merin S, Banin E, Sharon D.
    Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):3884-92. PubMed ID: 20220053
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  • 7. Association of acquired color vision defects in blue cone monochromatism.
    Terasaki H, Miyake Y.
    Jpn J Ophthalmol; 1995 Aug; 39(1):55-9. PubMed ID: 7643484
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  • 8. Cone signal contributions to electroretinograms [correction of electrograms] in dichromats and trichromats.
    Kremers J, Usui T, Scholl HP, Sharpe LT.
    Invest Ophthalmol Vis Sci; 1999 Apr; 40(5):920-30. PubMed ID: 10102289
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  • 10. Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.
    Michaelides M, Johnson S, Simunovic MP, Bradshaw K, Holder G, Mollon JD, Moore AT, Hunt DM.
    Eye (Lond); 2005 Jan; 19(1):2-10. PubMed ID: 15094734
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  • 12. Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A).
    Jiang L, Katz BJ, Yang Z, Zhao Y, Faulkner N, Hu J, Baird J, Baehr W, Creel DJ, Zhang K.
    Mol Vis; 2005 Feb 20; 11():143-51. PubMed ID: 15735604
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  • 13. The multifocal pattern electroretinogram (mfPERG) and cone-isolating stimuli.
    Langrová H, Jägle H, Zrenner E, Kurtenbach A.
    Vis Neurosci; 2007 Feb 20; 24(6):805-16. PubMed ID: 18093368
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  • 14. Macular dystrophy with protan genotype and phenotype studied with cone type specific ERGs.
    Scholl HP, Kremers J, Wissinger B.
    Curr Eye Res; 2001 Mar 20; 22(3):221-8. PubMed ID: 11462159
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  • 15. Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect.
    Hayashi T, Kubo A, Takeuchi T, Gekka T, Goto-Omoto S, Kitahara K.
    Vis Neurosci; 2006 Mar 20; 23(3-4):411-7. PubMed ID: 16961974
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  • 16. Cone dystrophies: clinical and electrophysiological findings.
    Kellner U, Kleine-Hartlage P, Foerster MH.
    Ger J Ophthalmol; 1992 Mar 20; 1(2):105-9. PubMed ID: 1477624
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  • 19. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2008 Feb 20; 49(2):751-7. PubMed ID: 18235024
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  • 20. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP.
    Hum Mutat; 2005 Mar 20; 25(3):248-58. PubMed ID: 15712225
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