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Journal Abstract Search

102 related items for PubMed ID: 13765544

  • 1. [Studies on the genetic carrier of color deficiency].
    MAJIMA A, AWAYA S, SHINOBU I, ICHIKAWA H.
    Rinsho Ganka; 1961 Feb; 15():161-8. PubMed ID: 13765544
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  • 3. Linkage between deficiency of glucose-6-phosphate dehydrogenase and colour-blindness.
    ADAM A.
    Nature; 1961 Feb 25; 189():686. PubMed ID: 13681296
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  • 4. [Quantitative test of color vision in healthy Chinese and genetic carriers of color deficiency].
    Chang J.
    Zhonghua Yan Ke Za Zhi; 1982 Jul 25; 18(4):242-4. PubMed ID: 6816554
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  • 9. [Color blindness (daltonism) in the light of genetic studies].
    Goncerzewicz M, Krawczyński M, Suchocka-Luczak S.
    Wiad Lek; 1971 Feb 15; 24(4):337-42. PubMed ID: 4929739
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  • 11. The molecular genetics of color vision and color blindness.
    Piantanida T.
    Trends Genet; 1988 Nov 15; 4(11):319-23. PubMed ID: 2907192
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  • 13. [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 Nov 15; 86(6):601-6. PubMed ID: 6982608
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  • 14. [STUDIES ON GENETIC CARRIERS OF COLOR DEFICIENCIES. 4. RESULTS OF A SATURATION DISCRIMINATION TEST].
    MAJIMA A, WATANABE B.
    Rinsho Ganka; 1963 Nov 15; 17():544-50. PubMed ID: 14130624
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  • 15. [Color vision of a repulsion compound heterozygote and her sons. Psychophysical and electroretinographic studies].
    Hanazaki H, Nakazato H, Tanabe J, Kawasaki K, Yonemura D.
    Nippon Ganka Gakkai Zasshi; 1987 May 15; 91(5):553-8. PubMed ID: 3499059
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  • 16. Linkage of color blindness to hemophilias A and B.
    WHITTAKER DL, COPELAND DL, GRAHAM JB.
    Am J Hum Genet; 1962 Jun 15; 14(2):149-58. PubMed ID: 14006651
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  • 17. THE RED-LIGHT ABSOLUTE THRESHOLD IN HETEROZYGOTE PROTAN CARRIERS. POSSIBLE GENETIC IMPLICATIONS.
    KRILL AE, BEUTLER E.
    Invest Ophthalmol; 1964 Feb 15; 3():107-18. PubMed ID: 14121141
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  • 18. Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness.
    Wu LZ, Zeng LH, Ma QY, Xie YJ, Chen YZ, Wu DZ.
    Jpn J Ophthalmol; 1988 Feb 15; 32(2):236-45. PubMed ID: 3263528
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  • 19. [Characteristics of genetic carriers of congenital color vision defects. (4) Detection of carriers (author's transl)].
    Yasuma T, Ichikawa H, Ichikawa K, Tanabe S.
    Nippon Ganka Gakkai Zasshi; 1981 May 10; 85(5):381-4. PubMed ID: 6973920
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