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Journal Abstract Search

113 related items for PubMed ID: 6982608

  • 1. [Characteristics of genetic carriers of congenital color vision defects. (5) Abnormalities of cone photopigments in proto-carriers].
    Yasuma T, Tokuda H.
    Nippon Ganka Gakkai Zasshi; 1982; 86(6):601-6. PubMed ID: 6982608
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  • 2. Four cone pigments in women heterozygous for color deficiency.
    Nagy AL, MacLeod DI, Heyneman NE, Eisner A.
    J Opt Soc Am; 1981 Jun; 71(6):719-22. PubMed ID: 6973012
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  • 3. The dimensionality of color vision in carriers of anomalous trichromacy.
    Jordan G, Deeb SS, Bosten JM, Mollon JD.
    J Vis; 2010 Jul 01; 10(8):12. PubMed ID: 20884587
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  • 6. Color discrimination in carriers of color deficiency.
    Hood SM, Mollon JD, Purves L, Jordan G.
    Vision Res; 2006 Sep 01; 46(18):2894-900. PubMed ID: 16690099
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  • 9. Rayleigh matches in carriers of inherited color vision defects: the contribution from the third L/M photopigment.
    Sun Y, Shevell SK.
    Vis Neurosci; 2008 Sep 01; 25(3):455-62. PubMed ID: 18598418
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  • 15. Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
    Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2007 May 01; 48(5):2362-70. PubMed ID: 17460303
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  • 16. [The properties of visual functions and familial analysis in blue cone monochromatism].
    Terasaki H, Miyake Y.
    Nippon Ganka Gakkai Zasshi; 1992 Apr 01; 96(4):523-30. PubMed ID: 1621595
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  • 17. [Blue cone monochromasia: diagnosis, genetic counseling and optical aids].
    Zrenner E, Magnussen S, Lorenz B.
    Klin Monbl Augenheilkd; 1988 Nov 01; 193(5):510-7. PubMed ID: 3264866
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