These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

151 related items for PubMed ID: 4548143

  • 1. Genealogical studies on interesting families of defective colour vision discovered by a mass examination in Japan and Formosa.
    Ichikawa H, Majima A.
    Mod Probl Ophthalmol; 1974; 13(0):265-71. PubMed ID: 4548143
    [No Abstract] [Full Text] [Related]

  • 2. Genetics and physiology of colour vision ("my story on colour vision genetics and physiology").
    Waaler GH.
    Acta Ophthalmol Suppl; 1973; ():1-75. PubMed ID: 4356807
    [No Abstract] [Full Text] [Related]

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

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

  • 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; 13(0):277-81. PubMed ID: 4548145
    [No Abstract] [Full Text] [Related]

  • 6. [Abnormal color vision in the light of examinations of school children].
    Goncerzewicz M, Krawczyński M, Suchocka-Luczak S.
    Pediatr Pol; 1971 Mar; 46(3):327-31. PubMed ID: 5314000
    [No Abstract] [Full Text] [Related]

  • 7. Two different alleles for deuteranomaly within a family with Leber's optic atrophy.
    Grützner P, Schrapp A.
    Mod Probl Ophthalmol; 1974 Mar; 13(0):258-61. PubMed ID: 4548141
    [No Abstract] [Full Text] [Related]

  • 8. [Early detection of color blindness from the viewpoint of occupational medicine with various references to internistic and human genetic symptom complexes].
    Ebéné RT.
    Fortschr Med; 1983 Jan 20; 101(3):51-4. PubMed ID: 6600702
    [Abstract] [Full Text] [Related]

  • 9. 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 Jan 20; 13(0):272-6. PubMed ID: 4548144
    [No Abstract] [Full Text] [Related]

  • 10. Practical problems of defective colour vision.
    Taylor WO.
    Practitioner; 1975 May 20; 214(1283):654-660. PubMed ID: 1079942
    [No Abstract] [Full Text] [Related]

  • 11. The heredity of normal and defective colour vision.
    Waaler GH.
    Acta Ophthalmol (Copenh); 1968 May 20; 46(1):33-40. PubMed ID: 5300920
    [No Abstract] [Full Text] [Related]

  • 12. 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 20; 48(5):2362-70. PubMed ID: 17460303
    [Abstract] [Full Text] [Related]

  • 13. Anomalous color vision in three Mexican populations.
    Halberstein RA, Crawford MH.
    Am J Phys Anthropol; 1974 Jul 20; 41(1):91-4. PubMed ID: 4546347
    [No Abstract] [Full Text] [Related]

  • 14. Colour blindness--a rural prevalence survey.
    Natu M.
    Indian J Ophthalmol; 1987 Jul 20; 35(2):71-3. PubMed ID: 3502467
    [No Abstract] [Full Text] [Related]

  • 15. Data concerning colour vision deficiencies amongst 29,985 young Greeks.
    Koliopoulos J, Iordanides P, Palmeris G, Chimonidou E.
    Mod Probl Ophthalmol; 1976 Jul 20; 17():161-4. PubMed ID: 1085863
    [Abstract] [Full Text] [Related]

  • 16. [Genetic studies on defective color vision in junior high school students. 2. Examinations on pedigrees with color vision defectives].
    Ichikawa H, Majima A, Komatsu S, Tokita H.
    Nippon Ganka Gakkai Zasshi; 1970 Sep 20; 74(9):1206-10. PubMed ID: 5312086
    [No Abstract] [Full Text] [Related]

  • 17. [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 Sep 20; 92():336-44. PubMed ID: 6971685
    [No Abstract] [Full Text] [Related]

  • 18. [Dyschromatopsy in twins].
    Kloucek F, Kubicková Z.
    Sb Lek; 1971 Mar 20; 73(3):57-63. PubMed ID: 5313898
    [No Abstract] [Full Text] [Related]

  • 19. What should the physician know about color vision?
    Linksz A.
    Proc Rudolf Virchow Med Soc City N Y; 1965 Mar 20; 24():1-7. PubMed ID: 5307774
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.