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 ...
AbstractLarge-field Rayleigh match ranges were measured in 27 red/green color-deficient male observe...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeuteranomalous trichromacy is the most common form of inherited color-vision deficiency. A ...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeutan observers are a heterogeneous group, varying nearly continuously from deuteranomalous...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
AbstractThe goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-d...
We have examined the colour vision of 43 female subjects in the age range 30-59 yr of whom 31 were o...
Background: The prevalence of congenital color vision defects (CCVD) is reported to be approximately...
AbstractMany subjects despite having only a single X-linked pigment gene (single-L/M-gene subjects) ...
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...
Some 12% of women are carriers of the mild, X-linked forms of color vision deficiencies called "anom...
AbstractLarge-field Rayleigh match ranges were measured in 27 red/green color-deficient male observe...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeuteranomalous trichromacy is the most common form of inherited color-vision deficiency. A ...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeutan observers are a heterogeneous group, varying nearly continuously from deuteranomalous...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
AbstractThe goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-d...
We have examined the colour vision of 43 female subjects in the age range 30-59 yr of whom 31 were o...
Background: The prevalence of congenital color vision defects (CCVD) is reported to be approximately...
AbstractMany subjects despite having only a single X-linked pigment gene (single-L/M-gene subjects) ...
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...
Some 12% of women are carriers of the mild, X-linked forms of color vision deficiencies called "anom...
AbstractLarge-field Rayleigh match ranges were measured in 27 red/green color-deficient male observe...
AbstractIndividual differences in abnormal color vision are well known. A fundamental unresolved pro...
AbstractDeuteranomalous trichromacy is the most common form of inherited color-vision deficiency. A ...