X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (8536) 8536
Book Review (1606) 1606
Publication (826) 826
Book / eBook (821) 821
Magazine Article (134) 134
Book Chapter (69) 69
Newspaper Article (34) 34
Newsletter (31) 31
Conference Proceeding (29) 29
Government Document (15) 15
Trade Publication Article (11) 11
Dissertation (9) 9
Patent (7) 7
Data Set (3) 3
Reference (3) 3
Paper (1) 1
Presentation (1) 1
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (6722) 6722
humans (6126) 6126
ophthalmology (4439) 4439
male (4040) 4040
female (3997) 3997
eye diseases (3331) 3331
middle aged (2513) 2513
adult (2288) 2288
eye (2136) 2136
aged (2015) 2015
genetic structures (1616) 1616
sense organs (1487) 1487
diagnosis (1230) 1230
research (1148) 1148
child (1085) 1085
risk factors (1051) 1051
adolescent (1043) 1043
retina (996) 996
surgery (954) 954
glaucoma (953) 953
aged, 80 and over (940) 940
care and treatment (909) 909
prevalence (900) 900
analysis (877) 877
abridged index medicus (821) 821
eyes (778) 778
macular degeneration (776) 776
animals (770) 770
patients (760) 760
medicine (755) 755
child, preschool (734) 734
retrospective studies (715) 715
age (699) 699
research article (668) 668
studies (658) 658
visual acuity (651) 651
optical coherence tomography (643) 643
diabetic retinopathy (641) 641
neurosciences (640) 640
disease (633) 633
infant (619) 619
medicine & public health (605) 605
eye movements (597) 597
young adult (576) 576
prospective studies (557) 557
diseases (543) 543
physiological aspects (536) 536
multidisciplinary sciences (529) 529
article (528) 528
health aspects (526) 526
classification (517) 517
medical imaging (508) 508
follow-up studies (507) 507
pediatrics (500) 500
cross-sectional studies (497) 497
children (494) 494
diabetes (481) 481
mutation (477) 477
clinical neurology (475) 475
usage (468) 468
medical research (464) 464
tomography (463) 463
population (450) 450
cornea (429) 429
science (423) 423
abnormalities (412) 412
infant, newborn (408) 408
genetic aspects (394) 394
risk-factors (381) 381
tomography, optical coherence (380) 380
blindness (362) 362
epidemiology (361) 361
medicine, experimental (360) 360
visual acuity - physiology (352) 352
magnetic resonance imaging (351) 351
open-angle glaucoma (347) 347
cataracts (340) 340
review (339) 339
intraocular pressure (335) 335
treatment outcome (333) 333
genetics & heredity (329) 329
retinopathy (327) 327
development and progression (326) 326
genetics (324) 324
cataract (322) 322
fluorescein angiography (320) 320
methods (314) 314
psychiatry (314) 314
diagnosis, differential (313) 313
prognosis (308) 308
case-control studies (304) 304
phenotype (302) 302
neurology (301) 301
dry eye (300) 300
visual impairment (299) 299
hypertension (298) 298
pathology (290) 290
vision (282) 282
eyes & eyesight (276) 276
therapy (275) 275
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (692) 692
Collection Dvlpm't (Acquisitions) - Closed Orders (26) 26
Collection Dvlpm't (Acquisitions) - Vendor file (23) 23
Online Resources - Online (15) 15
UTL at Downsview - May be requested (13) 13
Robarts - Stacks (12) 12
St. Michael's Hospital - Stacks (10) 10
UofT at Mississauga - Stacks (8) 8
OISE - Stacks (5) 5
Scarborough Hospital - General (5) 5
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (5) 5
UofT at Scarborough - Stacks (5) 5
Scarborough Hospital - Birchmount (4) 4
Gerstein Science - Circulation Desk (3) 3
Humber River Regional Hospital - Finch Stacks (3) 3
Markham Stouffville Hospital - Stacks (3) 3
Providence Healthcare - Stacks (3) 3
Gerstein Science - Not Returned (2) 2
Gerstein Science - Reference (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
St Josephs Health Centre - Stacks (2) 2
Gerstein Science - Missing (1) 1
Gerstein Science - Periodical Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Lakeridge Health Sciences - Online (1) 1
Mt Sinai Hospital - Online (1) 1
OISE - Missing (1) 1
OISE - Storage (1) 1
Providence Healthcare - Reference (1) 1
Royal Ontario Museum - Periodical Stacks (1) 1
Royal Ontario Museum - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
St. Michael's Hospital - Circulation Desk (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (9562) 9562
French (42) 42
German (28) 28
Spanish (18) 18
Turkish (12) 12
Italian (6) 6
Chinese (5) 5
Japanese (5) 5
Arabic (4) 4
Korean (4) 4
Russian (3) 3
Dutch (2) 2
Greek (1) 1
Hungarian (1) 1
Latvian (1) 1
Slovenian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Bulletin de la Societe Belge d'Ophtalmologie, ISSN 0081-0746, 1985, Volume 216, pp. 59 - 68
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2015, Volume 97, Issue 1, pp. 99 - 110
Ablepharon macrostomia syndrome (AMS) and Barber-Say syndrome (BSS) are rare congenital ectodermal dysplasias characterized by similar clinical features. To... 
EPITHELIAL-MESENCHYMAL TRANSITION | FAMILIAL OCCURRENCE | SETLEIS SYNDROME | UNDIAGNOSED DISEASES | GENETICS & HEREDITY | MORPHOLOGY STANDARD TERMINOLOGY | SAETHRE-CHOTZEN SYNDROME | FRAMESHIFT MUTATION | ATROPHIC SKIN | TRANSCRIPTION FACTOR | AUTOSOMAL-DOMINANT INHERITANCE | Abnormalities, Multiple - pathology | Humans | Molecular Sequence Data | Hirsutism - pathology | Mutation, Missense - genetics | Chromatin Immunoprecipitation | Base Sequence | Hypertrichosis - pathology | Skin Abnormalities - pathology | Abnormalities, Multiple - genetics | Eyelid Diseases - genetics | Twist-Related Protein 1 - chemistry | Amino Acid Sequence | Eyelid Diseases - pathology | Repressor Proteins - chemistry | Hirsutism - genetics | Macrostomia - pathology | Hypertelorism - genetics | Models, Molecular | Repressor Proteins - genetics | Zebrafish | Hypertelorism - pathology | Macrostomia - genetics | Eye Abnormalities - genetics | Microscopy, Electron | Sequence Analysis, DNA | Exome - genetics | Phenotype | Animals | Hypertrichosis - genetics | Eye Abnormalities - pathology | Twist-Related Protein 1 - genetics | Protein Conformation | Skin Abnormalities - genetics | HeLa Cells | Physiological aspects | Genetic disorders | Gene mutations | Identification and classification | Genotype & phenotype | Correlation analysis | Amino acids | Mutation | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Journal Article
American Journal of Medical Genetics, ISSN 0148-7299, 1985, Volume 22, Issue 1, pp. 157 - 195
Lissencephaly (smooth brain) is an abnormality of brain development characterized by incomplete neuronal migration and a smooth cerebral surface. At least two... 
Facial Bones - abnormalities | Humans | Infant | Male | Brain - abnormalities | Muscular Dystrophies - genetics | Syndrome | Intellectual Disability - genetics | Eye Abnormalities | Abnormalities, Multiple - diagnosis | Skull - abnormalities | Female | Abnormalities, Multiple - classification | Abnormalities, Multiple - genetics | Index Medicus
Journal Article
Journal Article