Colour vision deficiencies thirteen, Volume 13
This volume contains 56 papers, which were selected after peer review and revision by the authors. The papers describe the latest developments in all aspects of research in colour vision deficiencies. There are seven sections, which cover recent advances in intraindividual differences, structures and functions in colour vision, acquired colour deficiencies, congenital colour deficiencies, and different aspects of tests and systems.
30 pages matching pigment genes in this book
Results 1-3 of 30
What people are saying - Write a review
We haven't found any reviews in the usual places.
Influence of lightness
Doctors with inherited colour
35 other sections not shown
1997 Kluwer Academic adapting field anomalous trichromacy anomalous trichromats axis background blue blue-yellow butterfly-shaped carriers chromatic discrimination chromatic sensitivity chromatic signals clinical colour contrast colour deficiency colour matching Colour Vision Deficiencies colour vision test cone input cone types desaturated detection deutan deuteranomalous deuteranopic diabetic dichromats Dordrecht dystrophy effect equation error scores Figure fovea foveal function green Ishihara lateral geniculate nucleus long-wave luminance macaque matching range measured mechanisms middle-wave midget ganglion cells modulation Mollon Moreland Nagel anomaloscope Neitz Normal Normal observers Ophthalmol opponent opsin optic neuritis optical density panel pathways patients pattern perimetry photopigments photoreceptor pigment genes Pinckers Pokorny Proc protan protanopia psychometric function psychophysical ratio Rayleigh match red-green response retina retinal pigment epithelium rod signals S-cone scotopic shown shows spatial spectral sensitivity stimulus subjects trichromats tritan unique yellow values VEPs Verriest Vision Res visual acuity visual field wavelength