UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3302) 3302
Newsletter (238) 238
Newspaper Article (179) 179
Book Chapter (80) 80
Dissertation (27) 27
Magazine Article (21) 21
Book / eBook (14) 14
Reference (12) 12
Conference Proceeding (4) 4
Web Resource (2) 2
Book Review (1) 1
Journal / eJournal (1) 1
Publication (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
prader-willi syndrome (2441) 2441
humans (2363) 2363
science & technology (2127) 2127
life sciences & biomedicine (2058) 2058
male (1517) 1517
female (1509) 1509
prader-willi syndrome - genetics (1464) 1464
child (930) 930
genetics & heredity (897) 897
adult (779) 779
adolescent (768) 768
child, preschool (630) 630
research (514) 514
prader-willi syndrome - diagnosis (485) 485
infant (428) 428
chromosomes, human, pair 15 (416) 416
obesity (408) 408
chromosome deletion (407) 407
prader–willi syndrome (406) 406
pediatrics (399) 399
angelman syndrome - genetics (393) 393
genomic imprinting (393) 393
medical research (372) 372
animals (362) 362
medicine, experimental (349) 349
prader-willi syndrome - complications (336) 336
phenotype (329) 329
prader-willi syndrome - physiopathology (328) 328
congenital, hereditary, and neonatal diseases and abnormalities (327) 327
chromosomes, human, pair 15 - genetics (310) 310
genetic aspects (310) 310
endocrinology & metabolism (309) 309
dna methylation (294) 294
genetics (292) 292
analysis (282) 282
nutritional and metabolic diseases (281) 281
genetic disorders (275) 275
neurosciences & neurology (275) 275
mice (244) 244
angelman syndrome (242) 242
social sciences (242) 242
children (239) 239
prader-willi syndrome - psychology (227) 227
chromosome 15 (218) 218
prader-willi syndrome - drug therapy (217) 217
prader‐willi syndrome (216) 216
young adult (212) 212
body mass index (203) 203
gene expression (202) 202
in situ hybridization, fluorescence (202) 202
middle aged (199) 199
infant, newborn (198) 198
abridged index medicus (196) 196
psychiatry (192) 192
biochemistry & molecular biology (185) 185
genes (180) 180
clinical neurology (179) 179
nervous system diseases (179) 179
uniparental disomy (178) 178
neurosciences (176) 176
chromosomes (175) 175
care and treatment (173) 173
prader-willi syndrome - pathology (167) 167
methylation (165) 165
prader-willi syndrome - metabolism (165) 165
karyotyping (160) 160
mental retardation (156) 156
chromosome mapping (154) 154
diagnosis (153) 153
rehabilitation (153) 153
autism (152) 152
somatotropin (152) 152
health aspects (151) 151
imprinting (150) 150
physiological aspects (143) 143
physical fitness (139) 139
chromosome aberrations (133) 133
growth hormone (133) 133
human growth hormone - therapeutic use (133) 133
risk factors (129) 129
hyperphagia (128) 128
intellectual disability - genetics (126) 126
body composition (125) 125
education & educational research (125) 125
education, special (125) 125
gene deletion (125) 125
genetic research (124) 124
prader-willi syndrome - blood (122) 122
psychology (121) 121
prader-willi (120) 120
research article (119) 119
prader-willi syndrome - epidemiology (117) 117
mutation (116) 116
base sequence (115) 115
behavior (115) 115
genotype (115) 115
polymerase chain reaction (115) 115
pedigree (112) 112
pregnancy (112) 112
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (7) 7
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Bindery (1) 1
Gerstein Science - Periodical Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Robarts - Stacks (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3682) 3682
French (45) 45
Japanese (38) 38
Chinese (36) 36
Spanish (33) 33
Portuguese (25) 25
German (17) 17
Polish (17) 17
Italian (11) 11
Russian (7) 7
Hungarian (5) 5
Korean (5) 5
Czech (4) 4
Danish (3) 3
Dutch (3) 3
Hebrew (2) 2
Norwegian (2) 2
Swedish (2) 2
Turkish (2) 2
Arabic (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American journal of obstetrics and gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
... recently added chromosomal microdeletion syndromes, have lagged behind. Thus, there is a continued need to educate clinicians and patients about the current benefits... 
amniocentesis | trisomy 13 | trisomy 21 | 47,XXY | noninvasive prenatal testing | noninvasive prenatal screening | 47,XXX | 47,XYY | cell-free DNA | NIPT | prenatal diagnosis | microdeletion syndrome | trisomy 18 | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Chromosome Disorders - blood | Predictive Value of Tests | Turner Syndrome - blood | Cri-du-Chat Syndrome - diagnosis | Humans | Angelman Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - genetics | Turner Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - blood | Trisomy 18 Syndrome - diagnosis | Cri-du-Chat Syndrome - genetics | Klinefelter Syndrome - blood | Klinefelter Syndrome - genetics | Sex Chromosome Aberrations | Microarray Analysis | Karyotyping | Down Syndrome - blood | Angelman Syndrome - genetics | Chorionic Villi Sampling | Chromosome Disorders - diagnosis | Prader-Willi Syndrome - genetics | Female | Down Syndrome - diagnosis | Amniocentesis | Prader-Willi Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Chromosomes, Human, X - genetics | Prader-Willi Syndrome - blood | Prenatal Diagnosis | In Situ Hybridization, Fluorescence | Cri-du-Chat Syndrome - blood | Pregnancy | Trisomy 18 Syndrome - blood | Sex Chromosome Disorders of Sex Development - diagnosis | Trisomy - diagnosis | Trisomy - genetics | Trisomy 13 Syndrome - blood | Cell-Free Nucleic Acids - blood | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Klinefelter Syndrome - diagnosis | Turner Syndrome - genetics | Angelman Syndrome - blood | Trisomy 13 Syndrome - diagnosis | Chromosome Disorders - genetics | DNA microarrays | Medical screening | Pregnant women | Chromosomes | Analysis | Index Medicus | Abridged Index Medicus
Journal Article
Journal of intellectual disability research, ISSN 1365-2788, 1992
Journal
PLoS genetics, ISSN 1553-7390, 05/2016, Volume 12, Issue 5, pp. e1005993 - e1005993
Journal Article
The journal of clinical endocrinology and metabolism, ISSN 1945-7197, 08/2017, Volume 102, Issue 8, pp. 3029 - 3039
Context: Only a few genetic causes for childhood obesity have been identified to date... 
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Hydrolases - genetics | Humans | DNA Repair Enzymes - genetics | Transcriptome | Child, Preschool | Male | Chromosome Duplication - genetics | RNA, Messenger - metabolism | Autoantigens - genetics | Case-Control Studies | DNA Copy Number Variations | Intellectual Disability - genetics | Young Adult | Chromosomes, Human, Pair 22 - genetics | Subcutaneous Fat - metabolism | Cell Cycle Proteins - genetics | Adult | Female | Chromosomes, Human, Pair 1 - genetics | Nuclear Proteins - genetics | Child | Microfilament Proteins - genetics | Abnormalities, Multiple - genetics | DiGeorge Syndrome - genetics | Chromosomes, Human, Pair 16 - genetics | Siblings | Autistic Disorder - genetics | Chromosome Deletion | Megalencephaly - genetics | Extracellular Matrix Proteins - genetics | Pediatric Obesity - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Proteins - genetics | Comparative Genomic Hybridization | Adolescent | Ataxia Telangiectasia Mutated Proteins - genetics | Kruppel-Like Transcription Factors - genetics | Acid Phosphatase - genetics | Chromosome Disorders - genetics | Obesity | Adipose tissue | Prader-Willi syndrome | Copy number | Genes | mRNA | Hybridization | Gene expression | Ribonucleic acid--RNA | Body mass index | DNA microarrays | Pathways | Clonal deletion | Body mass | Body size | Children | Age | Index Medicus | Abridged Index Medicus | deletions | insights | bardet-biedl-syndrome | association | Klinisk medicin | contributes | population | type-2 | Clinical Medicine | mutations | rearrangements | loci
Journal Article
American journal of human genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 555 - 566
Journal Article
Journal of the American Academy of Child and Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 8, pp. 794 - 809
.... Results Several genetic syndromes... 
Pediatrics | Psychiatry | autism spectrum disorders | epigenetics | genetics | Social Sciences | Life Sciences & Biomedicine | Psychology | Psychology, Developmental | Science & Technology | Autism | Etiology | Pervasive Developmental Disorders | Mental Retardation | Evidence | Genetics | Environmental Influences | Cognitive Development | Symptoms (Individual Disorders) | Megalencephaly - psychology | Angelman Syndrome - psychology | Humans | Rett Syndrome - psychology | Angelman Syndrome - diagnosis | Social Environment | CHARGE Syndrome - psychology | Turner Syndrome - diagnosis | Prader-Willi Syndrome - psychology | Child Development Disorders, Pervasive - diagnosis | Angelman Syndrome - genetics | Prader-Willi Syndrome - genetics | Child | Fragile X Syndrome - genetics | Genetic Predisposition to Disease - psychology | Megalencephaly - genetics | Prader-Willi Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Genetic Association Studies | Rett Syndrome - diagnosis | Comorbidity | Risk Factors | CHARGE Syndrome - diagnosis | Chromosomes, Human, Pair 15 - genetics | Megalencephaly - diagnosis | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | Epigenesis, Genetic - genetics | Fragile X Syndrome - psychology | Adolescent | Turner Syndrome - genetics | CHARGE Syndrome - genetics | Rett Syndrome - genetics | Fragile X Syndrome - diagnosis | Psychological aspects | Epigenetic inheritance | Genetic aspects | Epigenetics | Child psychology | Gene expression | Genomics | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
Journal Article