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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 16329753

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  • 2. Diagnosing protan heterozygosity using the Medmont C-100 colour vision test.
    Harris RW, Cole BL.
    Clin Exp Optom; 2005 Jul; 88(4):240-7. PubMed ID: 16083418
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  • 6. Phenotypic diagnosis of protan and deutan heterozygosity.
    Piantanida TP.
    Invest Ophthalmol; 1971 Dec; 10(12):979-84. PubMed ID: 5316078
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  • 7. 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; 48(5):2362-70. PubMed ID: 17460303
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  • 10. One of Australia's greatest cricketers was a protanope: a genetic detective story solved with the help of Schmidt's sign.
    Harris RW, Cole BL.
    Clin Exp Optom; 2005 Nov; 88(6):405-9. PubMed ID: 16329749
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  • 11. Performance of normal females and carriers of color-vision deficiencies on standard color-vision tests.
    Dees EW, Baraas RC.
    J Opt Soc Am A Opt Image Sci Vis; 2014 Apr 01; 31(4):A401-9. PubMed ID: 24695200
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  • 13. Abnormal colour vision is a handicap to playing cricket but not an insurmountable one.
    Harris RW, Cole BL.
    Clin Exp Optom; 2007 Nov 01; 90(6):451-6. PubMed ID: 17958568
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  • 14. Frequencies of protan and deutan alleles in some Israeli communities and a note on the selection-relaxation hypothesis.
    Adam A, Doron D, Modan R.
    Am J Phys Anthropol; 1967 May 01; 26(3):297-305. PubMed ID: 5298526
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  • 16. The new Richmond HRR pseudoisochromatic test for colour vision is better than the Ishihara test.
    Cole BL, Lian KY, Lakkis C.
    Clin Exp Optom; 2006 Mar 01; 89(2):73-80. PubMed ID: 16494609
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  • 17. [Hereditary color vision deficiency: Physiology, classification, diagnosis and application to aeronautics].
    Marechal M, Delbarre M, Berguiga M, Benisty D, Froussart-Maille F.
    J Fr Ophtalmol; 2019 Feb 01; 42(2):177-188. PubMed ID: 30704748
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