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PUBMED FOR HANDHELDS

Journal Abstract Search


70 related items for PubMed ID: 1085856

  • 1.
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  • 2. An informative large pedigree with four compound hemizygotes of three combinations of deutan and protan genes.
    Arias S, Rodríguez A.
    Acta Cient Venez; 1973; 24(2):44-52. PubMed ID: 4549004
    [No Abstract] [Full Text] [Related]

  • 3. Colour vision deficiencies and haemophilia.
    Jaeger W, Schneider VJ.
    Mod Probl Ophthalmol; 1976; 17():143-6. PubMed ID: 1085859
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  • 4. Color discrimination in carriers of color deficiency.
    Hood SM, Mollon JD, Purves L, Jordan G.
    Vision Res; 2006 Sep; 46(18):2894-900. PubMed ID: 16690099
    [Abstract] [Full Text] [Related]

  • 5. New families, one with two recombinants for estimation of recombination between the deutan and protan loci.
    Arias S, Rodríguez A.
    Humangenetik; 1972 Sep; 14(4):264-8. PubMed ID: 4538150
    [No Abstract] [Full Text] [Related]

  • 6. Chromaticity discrimination in protan and deutan heterozygotes.
    Verriest G.
    Mod Probl Ophthalmol; 1974 Sep; 13(0):262-4. PubMed ID: 4548142
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. Phenotypic diagnosis of protan and deutan heterozygosity.
    Piantanida TP.
    Invest Ophthalmol; 1971 Dec; 10(12):979-84. PubMed ID: 5316078
    [No Abstract] [Full Text] [Related]

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  • 10. Genetic hypotheses induced by unusual colour vision phenotypes.
    Arias S.
    Mod Probl Ophthalmol; 1976 Dec; 17():108-19. PubMed ID: 1085855
    [No Abstract] [Full Text] [Related]

  • 11. Red-green colour blindness in the Tormes-Alberche Valley (Avila-Central Spain).
    Cabrero FJ, Ortiz MA, Mesa MS, Fuster V, Moral P.
    Anthropol Anz; 1997 Dec; 55(3-4):295-301. PubMed ID: 9468757
    [Abstract] [Full Text] [Related]

  • 12. Genetics of colour vision.
    Went LN, de Vries-de Mol EC.
    Mod Probl Ophthalmol; 1976 Dec; 17():96-107. PubMed ID: 1085897
    [No Abstract] [Full Text] [Related]

  • 13. [The progeny of the two protan and deutan families described by Franceschetti and Klein (1949, 1956), one generation later. Genealogy, color vision and genomic DNA].
    Roth A, Klein D, Paccolat F, Hermès D, Pelizzone M, Mandel JL, Feil R.
    Ophtalmologie; 1989 Dec; 3(4):275-8. PubMed ID: 2641134
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  • 20. Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.
    Filippi G, Rinaldi A, Palmarino R, Seravalli E, Siniscalco M.
    Genetics; 1977 May; 86(1):199-212. PubMed ID: 301840
    [Abstract] [Full Text] [Related]


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