X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (385) 385
Publication (90) 90
Newspaper Article (54) 54
Book / eBook (16) 16
Book Review (11) 11
Magazine Article (7) 7
Book Chapter (5) 5
Patent (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (208) 208
humans (194) 194
genetics & heredity (179) 179
female (145) 145
male (134) 134
child (95) 95
child, preschool (94) 94
genetic aspects (81) 81
article (78) 78
research (75) 75
genetics (72) 72
mutation (70) 70
adolescent (67) 67
phenotype (67) 67
infant (63) 63
adult (57) 57
intellectual disability - genetics (51) 51
autism (50) 50
comparative genomic hybridization (49) 49
genes (49) 49
chromosome deletion (47) 47
genomics (47) 47
intellectual disability (47) 47
developmental disabilities - genetics (43) 43
animals (38) 38
developmental delay (38) 38
health aspects (37) 37
mutations (34) 34
proteins (33) 33
gene (32) 32
syndrome (32) 32
dna copy number variations (31) 31
risk factors (31) 31
young adult (31) 31
chromosomes (30) 30
diagnosis (30) 30
pedigree (30) 30
genetic variation (29) 29
report (29) 29
analysis (28) 28
gene deletion (28) 28
infant, newborn (28) 28
expression (27) 27
genetic disorders (27) 27
abnormalities, multiple - genetics (26) 26
microdeletion (26) 26
gene mutations (25) 25
mental-retardation (25) 25
physiological aspects (25) 25
epilepsy (24) 24
identification (24) 24
mice (24) 24
phenotypes (24) 24
seizures (24) 24
disease (23) 23
gene expression (23) 23
biochemistry & molecular biology (22) 22
genomes (22) 22
in situ hybridization, fluorescence (22) 22
mental retardation (22) 22
molecular sequence data (22) 22
deletion (21) 21
middle aged (21) 21
pediatrics (21) 21
medicine (20) 20
base sequence (19) 19
brain (19) 19
genetic association studies (19) 19
microdeletion syndrome (19) 19
clonal deletion (18) 18
genetic predisposition to disease (18) 18
intellectual disabilities (18) 18
microarray (18) 18
oligonucleotide array sequence analysis (18) 18
schizophrenia (18) 18
abridged index medicus (17) 17
amino acid sequence (17) 17
de-novo mutations (17) 17
disorders (17) 17
genotype & phenotype (17) 17
haploinsufficiency (17) 17
alleles (16) 16
chromosome disorders - genetics (16) 16
dna sequencing (16) 16
genome, human (16) 16
laboratories (16) 16
medical genetics (16) 16
medical research (16) 16
mutation - genetics (16) 16
nucleotide sequencing (16) 16
protein (16) 16
array cgh (15) 15
children (15) 15
copy number variation (15) 15
life sciences (15) 15
pregnancy (15) 15
seizures - genetics (15) 15
cohort studies (14) 14
cytogenetics (14) 14
medical colleges (14) 14
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (4) 4
Robarts - Stacks (4) 4
UTL at Downsview - May be requested (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
OISE - Stacks (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
Architecture Landscape (Shore + Moffat) - Oversize (1) 1
Art - Oversize (1) 1
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Faculty of Information - May be requested in 6-10 wks (1) 1
Online Resources - Online (1) 1
Toronto East General Hospital - Stacks (1) 1
UofT Schools - Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Genetics in Medicine, ISSN 1098-3600, 06/2013, Volume 15, Issue 6, pp. 478 - 481
Journal Article
Cell, ISSN 0092-8674, 07/2014, Volume 158, Issue 2, pp. 263 - 276
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 10, pp. 1063 - 1071
Journal Article
Cell, ISSN 0092-8674, 04/2012, Volume 149, Issue 3, pp. 525 - 537
Journal Article
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 03/2017, Volume 6, Issue 1, pp. 042 - 050
Abstract Chromosomal microarray (CMA) testing, used to identify DNA copy number variations (CNVs), has helped advance knowledge about genetics of human... 
Review Article | microarray | molecular cytogenetics | copy number variation | microduplication | microdeletion | Review | aCGH
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2012, Volume 367, Issue 14, pp. 1321 - 1331
Journal Article