AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild abnormalities of color matching and discrimination. In a sample of 55 carriers of protan and deutan deficiencies and 55 age-matched normal controls, we measured chromatic discrimination along a red-green axis. We found that discrimination was impaired in the case of carriers of deutan deficiencies (which affect the middle-wave-sensitive cones of the retina), but was normal in the case of carriers of protan deficiencies (which affect the long-wave-sensitive cones). We argue that this result can be explained by the difference in the relative numbers of middle- and long-wave cones in heterozygous retinae: the imbalance of the two cone types is ...
AbstractThe influence of congenital colour defects on a clinical computer test for equiluminous colo...
AbstractThe goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-d...
MEASUREMENTS were made of saturation discrimination of normal and colour defective subjects with ill...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
Background: The prevalence of congenital color vision defects (CCVD) is reported to be approximately...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
We have examined the colour vision of 43 female subjects in the age range 30-59 yr of whom 31 were o...
AbstractDeuteranomalous trichromacy is the most common form of inherited color-vision deficiency. A ...
AbstractThe Rayleigh match, a color match between a mixture of 545+670nm lights and 589nm light in m...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
Some 12% of women are carriers of the mild, X-linked forms of color vision deficiencies called "anom...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeutan observers are a heterogeneous group, varying nearly continuously from deuteranomalous...
PURPOSE. Leber's hereditary optic neuropathy (LHON) is a maternally inherited disease resulting...
We have used the Farnsworth-Munsell 100-hue (FM 100) test and Mollon-Reffin (MR) test to evaluate th...
AbstractThe influence of congenital colour defects on a clinical computer test for equiluminous colo...
AbstractThe goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-d...
MEASUREMENTS were made of saturation discrimination of normal and colour defective subjects with ill...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
Background: The prevalence of congenital color vision defects (CCVD) is reported to be approximately...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
We have examined the colour vision of 43 female subjects in the age range 30-59 yr of whom 31 were o...
AbstractDeuteranomalous trichromacy is the most common form of inherited color-vision deficiency. A ...
AbstractThe Rayleigh match, a color match between a mixture of 545+670nm lights and 589nm light in m...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
Some 12% of women are carriers of the mild, X-linked forms of color vision deficiencies called "anom...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeutan observers are a heterogeneous group, varying nearly continuously from deuteranomalous...
PURPOSE. Leber's hereditary optic neuropathy (LHON) is a maternally inherited disease resulting...
We have used the Farnsworth-Munsell 100-hue (FM 100) test and Mollon-Reffin (MR) test to evaluate th...
AbstractThe influence of congenital colour defects on a clinical computer test for equiluminous colo...
AbstractThe goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-d...
MEASUREMENTS were made of saturation discrimination of normal and colour defective subjects with ill...