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Journal Abstract Search

261 related items for PubMed ID: 6971685

  • 1. [Tritan type congenital anomalies and acquired color vision defects. Results of a genetic survey in an isolated group, the Kel Kummer].
    Roth A, Chaventré-Mano A, Chaventré A.
    Bull Mem Soc Fr Ophtalmol; 1980; 92():336-44. PubMed ID: 6971685
    [No Abstract] [Full Text] [Related]

  • 2. Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
    Went LN, Völker-Dieben H, de Vries-de Mol EC.
    Mod Probl Ophthalmol; 1974; 13(0):272-6. PubMed ID: 4548144
    [No Abstract] [Full Text] [Related]

  • 3. Colour vision in a pedigree with autosomal dominant optic atrophy.
    Ohba N, Imamura PM, Tanino T.
    Mod Probl Ophthalmol; 1976; 17():315-9. PubMed ID: 1085884
    [No Abstract] [Full Text] [Related]

  • 4. Comparison of the standard pseudoisochromatic plates--Parts 1 and 2--As screening tests for congenital red-green color vision deficiencies.
    Hovis JK, Cawker CL, Cranton D.
    J Am Optom Assoc; 1996 Jun; 67(6):320-6. PubMed ID: 8888852
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  • 5. Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy.
    Völker-Dieben HJ, Went LN, de Vries-de Mol EC.
    Mod Probl Ophthalmol; 1974 Jun; 13(0):277-81. PubMed ID: 4548145
    [No Abstract] [Full Text] [Related]

  • 6. A family with congenital deutan and tritan defects.
    Kinnear PR, Smith BR, Copland DR.
    Mod Probl Ophthalmol; 1976 Jun; 17():131-4. PubMed ID: 1085857
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  • 8. A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect.
    Gunther KL, Neitz J, Neitz M.
    Vis Neurosci; 2006 Jun; 23(3-4):403-9. PubMed ID: 16961973
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  • 15. [Intrafamilial association of complete and incomplete congenital achromatopsia with amblyopia and atypical (without amblyopia) of dominant autosomal transmission].
    Ponte F, Scialfa A.
    Ann Ottalmol Clin Ocul; 1968 Jun; 94(6):608-32. PubMed ID: 5312373
    [No Abstract] [Full Text] [Related]

  • 16. [The use of tritan plate and pseudoisochromatic tables for detection of colour vision disturbances (author's transl)].
    Trusiewiczowa D, Kordalewska A.
    Klin Oczna; 1980 Feb; 82(2):79-81. PubMed ID: 6966713
    [No Abstract] [Full Text] [Related]

  • 17. [Screening of congenital red-green color vision defects using pseudoisochromatic tables].
    Mäntyjärvi M, Leinonen M.
    Duodecim; 1990 Feb; 106(11):872-6. PubMed ID: 1670325
    [No Abstract] [Full Text] [Related]

  • 18. Results of the OSCAR test in groups of normal and abnormal subjects.
    Verriest G, Uvijls A.
    Bull Soc Belge Ophtalmol; 1986 Feb; 220():89-96. PubMed ID: 3502558
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  • 20. [Assessment of the panel D-15 and FM 100-hue tests for the detection of congenital dyschromatopsia].
    Huang SZ.
    Zhonghua Yan Ke Za Zhi; 1992 Nov; 28(6):338-40. PubMed ID: 1306466
    [No Abstract] [Full Text] [Related]

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