X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (31768) 31768
Book Review (4492) 4492
Publication (2176) 2176
Book / eBook (334) 334
Newspaper Article (285) 285
Book Chapter (211) 211
Newsletter (150) 150
Magazine Article (71) 71
Conference Proceeding (57) 57
Reference (32) 32
Web Resource (27) 27
Dissertation (24) 24
Trade Publication Article (12) 12
Government Document (10) 10
Paper (3) 3
Journal / eJournal (2) 2
Archival Material (1) 1
Presentation (1) 1
Transcript (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (27104) 27104
humans (25444) 25444
female (16895) 16895
male (14453) 14453
genetics & heredity (11756) 11756
adult (7820) 7820
chromosome aberrations (6696) 6696
karyotyping (6147) 6147
chromosomes (5733) 5733
child (4930) 4930
pregnancy (4837) 4837
chromosome deletion (4730) 4730
phenotype (4592) 4592
child, preschool (3934) 3934
animals (3924) 3924
in situ hybridization, fluorescence (3838) 3838
infant (3735) 3735
adolescent (3734) 3734
infant, newborn (3554) 3554
abnormalities, multiple - genetics (3552) 3552
mutation (3378) 3378
middle aged (3274) 3274
genetics (3257) 3257
genetic aspects (3106) 3106
genes (2841) 2841
syndrome (2748) 2748
chromosome disorders (2732) 2732
research (2698) 2698
obstetrics & gynecology (2607) 2607
trisomy (2561) 2561
oncology (2536) 2536
chromosome mapping (2510) 2510
analysis (2502) 2502
pedigree (2440) 2440
translocation, genetic (2437) 2437
gene (2334) 2334
mice (2128) 2128
aneuploidy (2080) 2080
pediatrics (2075) 2075
aged (2061) 2061
intellectual disability - genetics (2013) 2013
cytogenetics (2009) 2009
chromosome banding (1946) 1946
comparative genomic hybridization (1931) 1931
diagnosis (1931) 1931
abridged index medicus (1854) 1854
abnormalities (1850) 1850
prenatal diagnosis (1797) 1797
mosaicism (1787) 1787
mutations (1708) 1708
deletion (1637) 1637
biochemistry & molecular biology (1633) 1633
genomics (1584) 1584
cell biology (1572) 1572
genetic disorders (1514) 1514
genomes (1383) 1383
genetic research (1367) 1367
risk factors (1355) 1355
cancer (1354) 1354
dna (1315) 1315
expression (1295) 1295
gene expression (1257) 1257
children (1254) 1254
genotype (1220) 1220
anomalies (1206) 1206
article (1184) 1184
base sequence (1181) 1181
molecular sequence data (1171) 1171
x chromosome (1157) 1157
translocation (1146) 1146
in-situ hybridization (1140) 1140
fish (1138) 1138
gene deletion (1122) 1122
human genetics (1099) 1099
retrospective studies (1098) 1098
chromosome aberrations - genetics (1076) 1076
chromosome (1073) 1073
prognosis (1065) 1065
young adult (1050) 1050
deoxyribonucleic acid--dna (1035) 1035
mental-retardation (999) 999
research article (993) 993
karyotype (987) 987
medicine (987) 987
reproductive biology (987) 987
proteins (982) 982
mental retardation (972) 972
cytogenetic analysis (967) 967
ultrasonography, prenatal (961) 961
hematology (954) 954
genetic markers (952) 952
genetic linkage (912) 912
identification (900) 900
biotechnology & applied microbiology (871) 871
health aspects (860) 860
patients (854) 854
pathology (850) 850
polymerase chain reaction (849) 849
heart defects, congenital - genetics (842) 842
chromosome disorders - genetics (836) 836
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (276) 276
UTL at Downsview - May be requested (44) 44
UofT at Mississauga - Stacks (44) 44
UofT at Scarborough - Stacks (26) 26
Collection Dvlpm't (Acquisitions) - Closed Orders (21) 21
Collection Dvlpm't (Acquisitions) - Vendor file (14) 14
St. Michael's College (John M. Kelly) - 2nd Floor (14) 14
Online Resources - Online (12) 12
Law (Bora Laskin) - Stacks (7) 7
Royal Ontario Museum - Stacks (5) 5
Trinity College (John W Graham) - Stacks (5) 5
Victoria University E.J. Pratt - Stacks (5) 5
Earth Sciences (Noranda) - Stacks (4) 4
Robarts - Stacks (4) 4
St. Augustine's Seminary - Stacks (3) 3
UofT at Scarborough - Withdrawn (3) 3
Gerstein Science - Reference (2) 2
OISE - Stacks (2) 2
Regis College - Stacks (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Gerstein Science - Missing (1) 1
Holland Bloorview Kids Rehabilitation - Reference (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Law (Bora Laskin) - Law Faculty Library (1) 1
Mt Sinai Hospital - Pathology (1) 1
New College (Ivey) - Stacks (1) 1
OISE - Curriculum Resources (1) 1
Physics - Stacks (1) 1
Providence Healthcare - Stacks (1) 1
Scarborough Hospital - Birchmount (1) 1
Scarborough Hospital - General (1) 1
St Josephs Health Centre - Stacks (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
UofT at Scarborough - Bindery (1) 1
UofT at Scarborough - May be requested in 6-10 wks (1) 1
UofT at Scarborough - Sunnybrook Stacks (1) 1
Victoria University Emmanuel College - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (31041) 31041
French (693) 693
German (311) 311
Spanish (181) 181
Russian (139) 139
Japanese (92) 92
Italian (76) 76
Chinese (68) 68
Polish (49) 49
Portuguese (44) 44
Korean (33) 33
Hungarian (30) 30
Dutch (26) 26
Bulgarian (18) 18
Turkish (17) 17
Romanian (14) 14
Czech (11) 11
Slovak (9) 9
Hebrew (8) 8
Danish (7) 7
Ukrainian (7) 7
Serbian (6) 6
Croatian (5) 5
Swedish (5) 5
Slovenian (2) 2
Arabic (1) 1
Bosnian (1) 1
Catalan (1) 1
Finnish (1) 1
Latvian (1) 1
Lithuanian (1) 1
Norwegian (1) 1
Persian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal de pediatrie et de puericulture, ISSN 0987-7983, 11/2017, Volume 30, Issue 5-6, pp. 249 - 270
La cytogénétique médicale est née à la suite de la mise en évidence de la première anomalie chromosomique chez l’homme en 1959, la trisomie 21. Depuis, de... 
ACPA/CGH array | Caryotype | Anomalies chromosomiques | Trisomie | Conseil génétique
Journal Article
Journal de pediatrie et de puericulture, ISSN 0987-7983, 11/2017, Volume 30, Issue 5, p. 249
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.jpp.2017.09.007 
Cytogenetics | Chromosomes
Journal Article
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 04/2018, Volume 51, Issue 4, pp. 463 - 469
Journal Article
Journal Article
SPINE, ISSN 0362-2436, 07/2017, Volume 42, Issue 14, pp. E841 - E847
STUDY DESIGN.Retrospective study of a series of 286 patients with congenital scoliosis (CS). OBJECTIVE.To describe a large cohort of patients with CS and to... 
Scoliosis - genetics | Humans | Child, Preschool | Infant | Male | Young Adult | Scoliosis - complications | Algorithms | Adolescent | Chromosome Aberrations | Adult | Female | Retrospective Studies | Child | Scoliosis - congenital | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 1, pp. 36 - 45
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 06/2011, Volume 48, Issue 6, pp. 383 - 389
Journal Article