X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1845) 1845
Newspaper Article (659) 659
Publication (495) 495
Paper (408) 408
Book / eBook (363) 363
Dissertation (52) 52
Magazine Article (51) 51
Book Review (45) 45
Report (32) 32
Patent (29) 29
Book Chapter (27) 27
Web Resource (19) 19
Conference Proceeding (11) 11
Streaming Audio (7) 7
Trade Publication Article (6) 6
Reference (4) 4
Data Set (3) 3
Video Recording (2) 2
Electronic Resource (1) 1
Government Document (1) 1
Presentation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (519) 519
experiment (446) 446
particle physics (406) 406
index medicus (380) 380
physics - high energy physics - experiment (378) 378
physics (377) 377
high energy physics - experiment (363) 363
male (317) 317
female (313) 313
high energy physics (237) 237
hep (159) 159
adult (145) 145
animals (143) 143
genetics & heredity (143) 143
history (136) 136
particle physics - experiment (126) 126
ex (123) 123
phenomenology (122) 122
research (120) 120
middle aged (116) 116
nuclear experiment (112) 112
cern lhc coll (111) 111
analysis (106) 106
article (104) 104
[ phys.hexp ] physics [physics]/high energy physics - experiment [hep-ex] (103) 103
physical sciences (101) 101
experimental results (100) 100
p p: scattering (93) 93
[phys.hexp]physics [physics]/high energy physics - experiment [hep-ex] (89) 89
fysik (89) 89
physics of elementary particles and fields (87) 87
natural sciences (86) 86
naturvetenskap (86) 86
p p: colliding beams (86) 86
physics, particles & fields (82) 82
aged (81) 81
subatomär fysik (81) 81
child (80) 80
subatomic physics (80) 80
united states (75) 75
13000 gev-cms (74) 74
risk factors (71) 71
pedigree (67) 67
adolescent (62) 62
hadron-hadron scattering (62) 62
mutation (62) 62
cardiac & cardiovascular systems (60) 60
astrophysics (59) 59
health aspects (59) 59
intellectual disability - genetics (52) 52
pediatrics (52) 52
children (51) 51
infant, newborn (51) 51
child, preschool (49) 49
abridged index medicus (48) 48
astronomy & astrophysics (47) 47
electronic books (47) 47
genetic aspects (47) 47
genetics (47) 47
infant (47) 47
management (47) 47
pregnancy (47) 47
hep-ex (46) 46
mice (46) 46
studies (46) 46
syndrome (44) 44
gene (42) 42
phenotype (42) 42
science & technology (42) 42
autism (41) 41
biochemistry & molecular biology (41) 41
surgery (41) 41
mental retardation (40) 40
heart failure (39) 39
mental retardation, x-linked - genetics (39) 39
multidisciplinary sciences (38) 38
physiological aspects (38) 38
abnormalities, multiple - genetics (37) 37
elementary particles, quantum field theory (37) 37
prevalence (37) 37
quantum field theories, string theory (37) 37
time factors (37) 37
care and treatment (36) 36
mortality (36) 36
biography (35) 35
genes (35) 35
musical performances (35) 35
high energy astrophysical phenomena (34) 34
molecular sequence data (34) 34
neurosciences (34) 34
prevention (34) 34
chemistry (33) 33
professional hockey (33) 33
usage (33) 33
background (32) 32
ciências físicas [ciências naturais] (32) 32
ecology (32) 32
medicine (32) 32
brain (31) 31
education (31) 31
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (183) 183
UTL at Downsview - May be requested (77) 77
Victoria University E.J. Pratt - Stacks (38) 38
St. Michael's College (John M. Kelly) - 2nd Floor (32) 32
Thomas Fisher Rare Book - Rare Book (31) 31
Trinity College (John W Graham) - Stacks (30) 30
Online Resources - Online (25) 25
UofT at Mississauga - Stacks (24) 24
Gerstein Science - Stacks (23) 23
UofT at Scarborough - Stacks (23) 23
Collection Dvlpm't (Acquisitions) - Vendor file (22) 22
Pontifical Inst. Mediaeval Studies - Library use only (18) 18
OISE - Stacks (16) 16
Collection Dvlpm't (Acquisitions) - Closed Orders (10) 10
Engineering & Comp. Sci. - Stacks (9) 9
Trinity College (John W Graham) - Storage (9) 9
Royal Ontario Museum - Stacks (7) 7
Knox College (Caven) - Stacks (5) 5
Royal Ontario Museum - Far Eastern (5) 5
St. Michael's College (John M. Kelly) - 3rd Floor (5) 5
Earth Sciences (Noranda) - Stacks (4) 4
Robarts - Reference (4) 4
Victoria University E.J. Pratt - Reference (4) 4
Art - Library use only (3) 3
Music - Stacks (3) 3
Pontifical Inst. Mediaeval Studies - Guest (3) 3
St. Augustine's Seminary - Stacks (3) 3
University College (Laidlaw) - Stacks (3) 3
Criminology - Stacks (2) 2
Innis College - Stacks (2) 2
Law (Bora Laskin) - Stacks (2) 2
Media Commons - Audio Visual (2) 2
Thomas Fisher Rare Book - Reference (2) 2
Trinity College (John W Graham) - Reference (2) 2
Victoria University CRRS - Library use only (2) 2
Victoria University Emmanuel College - Stacks (2) 2
Art - Oversize (1) 1
Astronomy & Astrophysics - Ask at library (1) 1
Baycrest Hospital - Resident/Client Library (1) 1
Collection Dvlpm't (Acquisitions) - Rare Book (1) 1
Engineering & Comp. Sci. - Special Collections (1) 1
Faculty of Information - May be requested in 6-10 wks (1) 1
Faculty of Information - Stacks (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Media Commons - Library or classroom use (1) 1
Media Commons - Storage (1) 1
Music - Reference (1) 1
OISE - Curriculum Resources (1) 1
Pontifical Inst. Mediaeval Studies - Reference (1) 1
Regis College - Stacks (1) 1
Robarts - Government Pubs (1) 1
Robarts - Library use only (1) 1
Robarts - Not Returned (1) 1
Robarts - Storage (1) 1
Royal Ontario Museum - Rare Book (1) 1
Royal Ontario Museum - Reference Desk (1) 1
St. Michael's College (John M. Kelly) - Audio Visual (1) 1
Trinity College (John W Graham) - Churchill (1) 1
Trinity College (John W Graham) - Oversize (1) 1
Trinity College (John W Graham) - Rare Book (1) 1
United Church of Canada Archives - Archives (1) 1
University College (Laidlaw) - Purdy (1) 1
UofT Schools - Reference (1) 1
UofT Schools - Special Collections (1) 1
UofT at Mississauga - 1st Floor (1) 1
UofT at Mississauga - Reference (1) 1
Victoria University E.J. Pratt - EJ Pratt (1) 1
Victoria University E.J. Pratt - Storage (1) 1
Victoria University Emmanuel College - Storage (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3117) 3117
French (26) 26
German (9) 9
Latin (7) 7
Portuguese (5) 5
Spanish (5) 5
Italian (2) 2
Dutch (1) 1
Hebrew (1) 1
Romanian (1) 1
Vietnamese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2006, 2nd ed., Oxford monographs on medical genetics, ISBN 0195165683, Volume no. 52., xiv, 1495
Book
2000, Oxford monographs on medical genetics, ISBN 0195129814, Volume no. 39., xiii, 422
Book
2006, 2nd ed., Oxford monographs on medical genetics, ISBN 9780195165685, Volume no. 52
Web Resource
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2018, Volume 176, Issue 9, pp. 1968 - 1971
Random mating in the general population tends to limit the occurrence of homozygous and compound heterozygous forms of dominant hereditary disorders. Certain... 
arthrogryposis | compound heterozygosity | Waardenburg syndrome | SOX10 | biallelic deletion | GENETICS & HEREDITY | MUTATIONS | INHERITANCE | PRENATAL-DIAGNOSIS | Deafness | Dysplasia | Genes | Mating | Microphthalmia-associated transcription factor | Assortative mating | Phenotypes | Fetuses | Arthrogryposis | Pax3 protein | Sox10 protein | Genotypes | Cleft lip/palate | Hereditary diseases
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 06/2016, Volume 118, Issue 2, pp. 92 - 99
Journal Article
Clinical dysmorphology, ISSN 0962-8827, 01/2019, p. 1
Journal Article
EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 05/2014, Volume 22, Issue 5, pp. 594 - 601
Mucolipidosis (ML) II and ML III alpha/beta are allelic autosomal recessive metabolic disorders due to mutations in GNPTAB. The gene encodes the enzyme... 
mucolipidosis | storage disease | PSEUDO-HURLER POLYDYSTROPHY | ENZYME | GNPTAB | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | I-CELL DISEASE | OSTEODYSTROPHY | phosphotransferase
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 5, pp. 594 - 601
Journal Article
Clinical Dysmorphology, ISSN 0962-8827, 04/2019, Volume 28, Issue 2, pp. 71 - 73
Journal Article
Cancer Genetics, ISSN 2210-7762, 10/2018, Volume 226-227, pp. 53 - 54
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 04/2012, Volume 90, Issue 4, p. 579
X-Linked intellectual disability (XLID) accounts for 5%-10% of intellectual disability in males. Over 150 syndromes, the most common of which is the fragile X... 
Genomics | Genetics | Learning disabilities | Mutation | Medical diagnosis
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2015, Volume 52, Issue Suppl 1, pp. A2 - A3
BackgroundThe dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) gene on chromosome 21q22.13 within the Down syndrome critical region has... 
Journal Article
Cancer Genetics, ISSN 2210-7762, 05/2016, Volume 209, Issue 5, pp. 236 - 237
Journal Article
Cancer Genetics, ISSN 2210-7762, 2016, Volume 209, Issue 5, pp. 236 - 237
Journal Article
No results were found for your search.

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