Phenotypical variations of tritanopia
- 1 June 1966
- journal article
- research article
- Published by Elsevier in Vision Research
- Vol. 6 (5-6) , 301-313
- https://doi.org/10.1016/0042-6989(66)90064-2
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- The inheritance of congenital tritanopia with the report of an extensive pedigreeAnnals of Human Genetics, 1964
- On acquired deficiency of colour vision, with special reference to its detection and classification by means of the tests of FarnsworthVision Research, 1961
- Case of Congenital Tritanopia with Implications for a Trichromatic Model of Color Reception*Journal of the Optical Society of America, 1960
- Combined Forms of Congenital Colour Defects : A Pedigree with Atypical Total Colour BlindnessBritish Journal of Ophthalmology, 1956
- THE FAMILIAL DISTRIBUTION OF CONGENITAL TRITANOPIAAnnals of Human Genetics, 1955
- Some Quantitative Aspects of an Opponent-Colors Theory II Brightness, Saturation, and Hue in Normal and Dichromatic VisionJournal of the Optical Society of America, 1955
- The Characteristics of TritanopiaJournal of the Optical Society of America, 1952
- Spectral saturation and its relation to color-vision defects.Journal of Experimental Psychology, 1944
- Spektraluntersuchungen über die Minimalfeldhelligkeiten des Tritanomalen und seine Unterschiedsempfindlichkeit für Änderungen der HelligkeitAlbrecht von Graefes Archiv für Ophthalmologie, 1927
- Die Tritanomalie, ein bisher unbekannter Typus anomaler TrichromasieAlbrecht von Graefes Archiv für Ophthalmologie, 1925