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

123 related items for PubMed ID: 5298526

  • 1. 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; 26(3):297-305. PubMed ID: 5298526
    [No Abstract] [Full Text] [Related]

  • 2. Silent substitution tests like the OSCAR and the Medmont C100 can identify protan and deutan carriers of abnormal colour vision.
    Robbins HG.
    Clin Exp Optom; 2005 Nov; 88(6):426-7. PubMed ID: 16329753
    [No Abstract] [Full Text] [Related]

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

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [Evaluation of color pattern VECP in deutan].
    Tsukamoto M, Kakisu Y, Adachi-Usami E.
    Nippon Ganka Gakkai Zasshi; 1989 Oct; 93(10):993-1001. PubMed ID: 2603851
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. The incidence of red-green color deficiency in New Zealand's Maoris and "Islanders".
    Grosvenor T.
    Am J Optom Arch Am Acad Optom; 1970 Jun; 47(6):445-50. PubMed ID: 5310515
    [No Abstract] [Full Text] [Related]

  • 12. [Discrimination curve of color hues].
    Dubois-Poulsen A, Prévt-Paille G.
    Adv Ophthalmol; 1978 Jun; 36():149-63. PubMed ID: 307333
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [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 May; 3(4):275-8. PubMed ID: 2641134
    [Abstract] [Full Text] [Related]

  • 18. Ugandan colorblinds revisited.
    Adam A, Mwesigye E, Tabani E.
    Am J Phys Anthropol; 1970 Jan; 32(1):59-64. PubMed ID: 5309007
    [No Abstract] [Full Text] [Related]

  • 19. Anomaloscopic diagnoses of red-green blindness among Thais and Chinese.
    Adam A, Puenpatom M, Davivongs V, Wangspa S.
    Hum Hered; 1969 Jan; 19(5):509-13. PubMed ID: 5308426
    [No Abstract] [Full Text] [Related]

  • 20. Repeatability of the C-100 colour vision test.
    Hovis JK.
    Clin Exp Optom; 2003 May; 86(3):173-8. PubMed ID: 12767251
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.