X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (13) 13
index medicus (13) 13
female (10) 10
male (10) 10
adult (8) 8
middle aged (8) 8
ophthalmology (8) 8
aged (7) 7
adolescent (5) 5
pedigree (5) 5
retinitis pigmentosa - genetics (4) 4
visual acuity (4) 4
age (3) 3
aged, 80 and over (3) 3
check size (3) 3
child (3) 3
dna mutational analysis (3) 3
evoked potentials, visual - physiology (3) 3
genetics & heredity (3) 3
identification (3) 3
mutation - genetics (3) 3
phenotype (3) 3
abridged index medicus (2) 2
amino acid sequence (2) 2
amplitude (2) 2
atp-binding cassette transporters - genetics (2) 2
base sequence (2) 2
electroretinogram (2) 2
electroretinography (2) 2
evoked potentials, visual (2) 2
exons - genetics (2) 2
eyes (2) 2
follow-up studies (2) 2
genes, dominant (2) 2
genetic aspects (2) 2
genetic disorders (2) 2
genetic linkage (2) 2
genotype (2) 2
k su ophthalmology (2) 2
localization (2) 2
macula lutea (2) 2
macular dystrophy (2) 2
macular pucker (2) 2
molecular sequence data (2) 2
mutation (2) 2
night blindness - genetics (2) 2
recessive retinitis-pigmentosa (2) 2
research (2) 2
retinal degeneration - genetics (2) 2
retinal diseases (2) 2
retinal dystrophies (2) 2
retinal perforations (2) 2
retrospective studies (2) 2
rhodopsin gene (2) 2
rna, messenger - analysis (2) 2
stargardt-disease (2) 2
abcr (1) 1
abnormalities (1) 1
acid (1) 1
acoustic impedance tests (1) 1
age factors (1) 1
age-related maculopathy (1) 1
age-related-changes (1) 1
alcohol oxidoreductases - genetics (1) 1
animals (1) 1
atp-binding cassette transporters - chemistry (1) 1
audiometry, pure-tone (1) 1
auditory threshold (1) 1
auditory threshold - physiology (1) 1
autosomal recessive inheritance (1) 1
beaver dam eye (1) 1
binding protein (1) 1
capillaries (1) 1
carrier detection (1) 1
case-control studies (1) 1
cell (1) 1
cells, cultured (1) 1
chain alcohol dehydrogenases (1) 1
child, preschool (1) 1
choroid diseases (1) 1
choroid diseases - complications (1) 1
choroid diseases - diagnosis (1) 1
choroid diseases - genetics (1) 1
choroid diseases - physiopathology (1) 1
chromosome 17p (1) 1
chromosome 1p (1) 1
chromosome mapping - methods (1) 1
chromosome walking (1) 1
chromosome-11 (1) 1
chromosomes, human, pair 1 (1) 1
chromosomes, human, pair 1 - genetics (1) 1
chromosomes, human, pair 17 - genetics (1) 1
cloning, molecular - methods (1) 1
cofactor c (1) 1
color perception tests (1) 1
color perception tests - instrumentation (1) 1
color perception tests - methods (1) 1
color vision defects (1) 1
color vision defects - diagnosis (1) 1
color-vision (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 1999, Volume 64, Issue 4, pp. 1024 - 1035
Journal Article
Documenta Ophthalmologica, ISSN 0012-4486, 1995, Volume 90, Issue 3, pp. 247 - 257
Journal Article
Human Genetics, ISSN 0340-6717, 1999, Volume 104, Issue 1, pp. 73 - 76
Linkage analysis was performed on a large Dutch family with autosomal dominant retinitis pigmentosa. Linkage was found to the RP17 locus on chromosome 17q22,... 
RHODOPSIN GENE | LOCALIZATION | MUTATIONS | LOCUS | GENETICS & HEREDITY | Haplotypes | Humans | Retinitis Pigmentosa - genetics | Male | Genetic Markers | Chromosomes, Human, Pair 17 - genetics | Phenotype | Pedigree | Recombination, Genetic | Chromosome Mapping - methods | Female | Genes, Dominant - genetics | Genetic Linkage | Index Medicus
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 4/1998, Volume 236, Issue 5, pp. 326 - 332
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 01/1997, Volume 123, Issue 1, pp. 97 - 102
PURPOSE: To determine the extent of pattern-reversal visual evoked potential parameter alteration by epiretinal membranes and to investigate the use of... 
K SU OPHTHALMOLOGY | OPHTHALMOLOGY | EYES | MACULAR PUCKER | CHECK SIZE | AGE | Retina - physiology | Photic Stimulation - methods | Humans | Middle Aged | Evoked Potentials, Visual | Reaction Time | Visual Acuity | Membranes - physiology | Visual acuity | Abnormalities | Pattern recognition | Ophthalmology | Index Medicus | Abridged Index Medicus
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 1995, Volume 31, Issue 2, pp. 159 - 174
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 1976, Volume 82, Issue 4, pp. 540 - 548
An apparently autosomal-dominant macular dystrophy occurred in three pedigrees with the presenting sign of typical cystoid macular edema due to leaking... 
Electroretinography | Electrooculography | Macula Lutea | Edema - genetics | Retinal Degeneration - genetics | Humans | Middle Aged | Male | Genes, Dominant | Macular Degeneration - genetics | Pedigree | Adolescent | Adult | Female | Capillaries | Child
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 7/1999, Volume 237, Issue 8, pp. 629 - 635
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 8/1997, Volume 235, Issue 8, pp. 474 - 479
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.