X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (6986) 6986
Book Review (1193) 1193
Publication (965) 965
Newsletter (125) 125
Book Chapter (111) 111
Book / eBook (109) 109
Conference Proceeding (77) 77
Magazine Article (31) 31
Dissertation (9) 9
Newspaper Article (5) 5
Web Resource (5) 5
Presentation (2) 2
Data Set (1) 1
Reference (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (6039) 6039
humans (4616) 4616
ophthalmology (3351) 3351
male (2588) 2588
animals (2540) 2540
female (2464) 2464
retina (1990) 1990
retinal degeneration (1876) 1876
mutation (1845) 1845
adult (1554) 1554
eye diseases (1510) 1510
sense organs (1445) 1445
mice (1282) 1282
middle aged (1252) 1252
genetic structures (1225) 1225
retinal degeneration - genetics (1216) 1216
electroretinography (1180) 1180
macular degeneration (1115) 1115
pedigree (1065) 1065
genetics & heredity (1050) 1050
genetic aspects (953) 953
photoreceptors (947) 947
retinitis-pigmentosa (934) 934
child (884) 884
adolescent (864) 864
degeneration (856) 856
retinitis pigmentosa (819) 819
biochemistry & molecular biology (811) 811
aged (779) 779
phenotype (777) 777
research (764) 764
article (731) 731
eye proteins - genetics (725) 725
mutations (700) 700
gene (659) 659
disease models, animal (640) 640
analysis (638) 638
fluorescein angiography (638) 638
disease (626) 626
research article (609) 609
retinitis pigmentosa - genetics (603) 603
retina - pathology (597) 597
dystrophy (596) 596
genetics (585) 585
retinal degeneration - pathology (584) 584
leber congenital amaurosis (579) 579
visual acuity (573) 573
dna mutational analysis (559) 559
medicine (557) 557
genes (556) 556
neurosciences (554) 554
proteins (554) 554
retinal diseases - genetics (538) 538
retinal pigment epithelium (536) 536
cell biology (531) 531
physiological aspects (531) 531
tomography, optical coherence (528) 528
multidisciplinary sciences (518) 518
fundus oculi (516) 516
retina - metabolism (499) 499
blindness (490) 490
gene expression (479) 479
rats (471) 471
macular degeneration - genetics (457) 457
optical coherence tomography (444) 444
retinal dystrophy (443) 443
child, preschool (439) 439
abridged index medicus (438) 438
young adult (436) 436
gene therapy (430) 430
retinal diseases (420) 420
medicine, research & experimental (414) 414
molecular sequence data (414) 414
eye (412) 412
retinal-pigment epithelium (409) 409
expression (408) 408
diagnosis (403) 403
care and treatment (391) 391
retinal degeneration - physiopathology (384) 384
mice, inbred c57bl (376) 376
polymerase chain reaction (374) 374
genotype (361) 361
age (359) 359
science (349) 349
cone-rod dystrophy (345) 345
apoptosis (328) 328
retinal degeneration - metabolism (319) 319
health aspects (316) 316
base sequence (314) 314
amino acid sequence (304) 304
mice, knockout (302) 302
protein (302) 302
patients (298) 298
medicine & public health (296) 296
cells (289) 289
gene mutations (288) 288
biology (285) 285
light (282) 282
mouse model (281) 281
medical research (275) 275
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (72) 72
Online Resources - Online (7) 7
Collection Dvlpm't (Acquisitions) - Vendor file (6) 6
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
St. Michael's Hospital - Stacks (2) 2
Gerstein Science - Circulation Desk (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Providence Healthcare - Stacks (1) 1
Robarts - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (7120) 7120
German (95) 95
French (44) 44
Russian (16) 16
Spanish (14) 14
Japanese (6) 6
Polish (6) 6
Chinese (5) 5
Czech (5) 5
Portuguese (5) 5
Turkish (5) 5
Romanian (4) 4
Dutch (3) 3
Hungarian (2) 2
Slovak (2) 2
Catalan (1) 1
Italian (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 1, pp. 99 - 104
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e65574 - e65574
Background: Retinal dystrophies (RD) are a group of hereditary diseases that lead to debilitating visual impairment and are usually transmitted as a Mendelian... 
LEBER CONGENITAL AMAUROSIS | RP1 | GENE | USHER-SYNDROME | MULTIDISCIPLINARY SCIENCES | RECESSIVE RETINITIS-PIGMENTOSA | GENOTYPING MICROARRAY | MODIFIER ALLELES | MUTATIONS | IDENTIFICATION | SPANISH FAMILIES | Genetic Predisposition to Disease - genetics | Extracellular Matrix Proteins - genetics | Humans | Cyclic Nucleotide-Gated Cation Channels - genetics | Retinitis Pigmentosa - genetics | Male | Leber Congenital Amaurosis - genetics | Spain | Exome - genetics | ATP-Binding Cassette Transporters - genetics | Usher Syndromes - genetics | Pedigree | Adaptor Proteins, Signal Transducing - genetics | Nicotinamide-Nucleotide Adenylyltransferase - genetics | Female | Eye Proteins - genetics | Retinal Dystrophies - genetics | Genetic aspects | Genetic disorders | Disease transmission | Nucleotide sequencing | Genes | DNA sequencing | USH2A protein | Retinitis pigmentosa | Retina | Identification | Genomes | Hybridization | Medical diagnosis | Gene sequencing | Genetics | Diagnosis | Genotypes | Deoxyribonucleic acid--DNA | Visually handicapped people | Data analysis | Congenital diseases | Data processing | Patients | Hereditary diseases | Studies | Blindness | Acetylcholine receptors | Diagnostic systems | Retinitis | Mutation | Dystrophy | Genetic testing | Cost analysis | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 10/2017, Volume 182, pp. 81 - 89
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, pp. e78496 - e78496
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2016, Volume 11, Issue 1, pp. e0145951 - e0145951
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2016, Volume 99, Issue 2, pp. 470 - 480
Journal Article