X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (32) 32
male (25) 25
ophthalmology (24) 24
blue cone monochromacy (23) 23
female (19) 19
index medicus (19) 19
color vision defects - genetics (17) 17
achromatopsia (15) 15
molecular-genetics (14) 14
blue (13) 13
color vision (13) 13
neurosciences (13) 13
genetics & heredity (12) 12
pedigree (12) 12
adult (10) 10
electroretinography (10) 10
mutation (10) 10
adolescent (9) 9
animals (9) 9
genes (9) 9
genetics (9) 9
mutations (9) 9
retinal cone photoreceptor cells - physiology (9) 9
child (8) 8
human red (8) 8
middle aged (8) 8
phenotype (8) 8
retina (8) 8
blue-cone monochromacy (7) 7
green (7) 7
human color-vision (7) 7
vision (7) 7
visual pigments (7) 7
child, preschool (6) 6
color vision defects - physiopathology (6) 6
genetic aspects (6) 6
genetic structures (6) 6
polymerase chain reaction (6) 6
research (6) 6
young adult (6) 6
analysis (5) 5
article (5) 5
blue-sensitive cones (5) 5
chromosome mapping (5) 5
color blindness (5) 5
color-vision (5) 5
colour vision (5) 5
cone dystrophy (5) 5
cones (5) 5
eye diseases (5) 5
gene (5) 5
genotype (5) 5
molecular sequence data (5) 5
photoreceptors (5) 5
pigments (5) 5
retinal dystrophy (5) 5
sense organs (5) 5
spectral sensitivity (5) 5
x chromosome (5) 5
alpha-subunit (4) 4
chromosomes, human, x - genetics (4) 4
color perception - genetics (4) 4
color perception - physiology (4) 4
cone opsins - genetics (4) 4
discrimination (4) 4
gene deletion (4) 4
genetic diseases, x-linked - genetics (4) 4
heterozygote (4) 4
opsin (4) 4
protan (4) 4
red (4) 4
retinitis pigmentosa - genetics (4) 4
rod opsins - genetics (4) 4
rods (4) 4
visual pigment genes (4) 4
aged (3) 3
amino acid sequence (3) 3
aphakia (3) 3
array (3) 3
base sequence (3) 3
biochemistry & molecular biology (3) 3
blue cone monochromatism (3) 3
chromosomes (3) 3
color vision defects - therapy (3) 3
color-vision deficiencies (3) 3
colour vision deficiency (3) 3
cone-rod dystrophy (3) 3
cut-off filter (3) 3
deutan (3) 3
dna (3) 3
dna microarrays (3) 3
driving ability (3) 3
expression (3) 3
gene mutations (3) 3
genetic disorders (3) 3
genetic linkage (3) 3
leber congenital amaurosis (3) 3
light (3) 3
locus-control region (3) 3
monochromacy (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Ophthalmic Genetics, ISSN 1381-6810, 01/2019, Volume 40, Issue 1, pp. 43 - 48
Background: To clarify the diagnosis of a Chinese patient with novel double heterozygous in the NR2E3 and OPN1LW genes and describe the clinical features.... 
enhanced S-cone syndrome | OPN1LW gene | Blue cone monochromacy | NR2E3 gene | OPHTHALMOLOGY | NR2E3 | GENETICS & HEREDITY
Journal Article
Naturwissenschaften, ISSN 0028-1042, 3/2011, Volume 98, Issue 3, pp. 193 - 201
Journal Article
Ophthalmologe, ISSN 0941-293X, 11/2018, Volume 115, Issue 11, pp. 916 - 921
Journal Article
Human Mutation, ISSN 1059-7794, 11/2014, Volume 35, Issue 11, pp. 1354 - 1362
Journal Article
OPHTHALMOLOGE, ISSN 0941-293X, 11/2018, Volume 115, Issue 11, pp. 916 - 921
Edge filters are used in aphakic eyes as asubstitute of the natural cut-off filter of the intact eye or in other causes of a lack of light absorption in the... 
Aphakia | Blue cone monochromacy | Driving ability | LOW-VISION | OPHTHALMOLOGY | AIDS | Achromatopsia | Retinal dystrophy | Cut-off filter (edge filter) | Retina | Filtration | Glare | Humans | Adaptation, Ocular | Retinal Dystrophies
Journal Article
Der Ophthalmologe, ISSN 0941-293X, 11/2018, Volume 115, Issue 11, pp. 916 - 921
Kantenfilter dienen zum einen als Ersatz der natürlichen Kantenfilterfunktion im Auge wie bei Aphakie oder anderen Ursachen einer fehlenden Lichtabsorption im... 
Aphakia | Kraftfahreignung | Aphakie | Blue cone monochromacy | Kantenfilter | Achromatopsia | Achromatopsie | Blauzapfenmonochromasie | Netzhautdystrophie | Medicine & Public Health | Driving ability | Ophthalmology | Retinal dystrophy | Cut-off filter (edge filter)
Journal Article
HUMAN MOLECULAR GENETICS, ISSN 0964-6906, 05/2002, Volume 11, Issue 10, pp. 1219 - 1227
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 01/2013, Volume 161, Issue 1, pp. 120 - 130
Journal Article