X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (6229) 6229
Publication (646) 646
Newsletter (289) 289
Newspaper Article (150) 150
Book Chapter (135) 135
Book Review (54) 54
Dissertation (51) 51
Conference Proceeding (34) 34
Magazine Article (34) 34
Book / eBook (23) 23
Reference (15) 15
Web Resource (9) 9
Journal / eJournal (5) 5
Trade Publication Article (3) 3
Transcript (2) 2
Streaming Video (1) 1
Video Recording (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (4207) 4207
prader-willi syndrome (3417) 3417
male (2484) 2484
female (2457) 2457
index medicus (1791) 1791
prader-willi-syndrome (1669) 1669
child (1559) 1559
prader-willi syndrome - genetics (1448) 1448
genetics & heredity (1443) 1443
adult (1241) 1241
adolescent (1213) 1213
child, preschool (964) 964
animals (892) 892
children (840) 840
obesity (817) 817
research (711) 711
pediatrics (699) 699
genomic imprinting (669) 669
phenotype (618) 618
infant (617) 617
endocrinology & metabolism (616) 616
dna methylation (595) 595
prader-willi syndrome - diagnosis (559) 559
mice (547) 547
chromosomes, human, pair 15 (535) 535
angelman syndrome - genetics (521) 521
prader-willi syndrome - complications (519) 519
chromosome deletion (481) 481
angelman syndrome (467) 467
prader-willi (461) 461
medical research (458) 458
analysis (449) 449
genetics (443) 443
prader-willi syndrome - physiopathology (443) 443
medicine, experimental (438) 438
genetic aspects (426) 426
uniparental disomy (414) 414
biochemistry & molecular biology (409) 409
neurosciences (403) 403
prader–willi syndrome (403) 403
diagnosis (402) 402
chromosomes, human, pair 15 - genetics (394) 394
autism (348) 348
deletion (346) 346
prader-willi syndrome - drug therapy (333) 333
methylation (327) 327
adults (325) 325
psychiatry (323) 323
gene (321) 321
infant, newborn (312) 312
genetic disorders (310) 310
congenital, hereditary, and neonatal diseases and abnormalities (309) 309
middle aged (309) 309
article (305) 305
gene expression (303) 303
in situ hybridization, fluorescence (301) 301
clinical neurology (297) 297
genes (296) 296
mental retardation (294) 294
young adult (291) 291
behavior (288) 288
body mass index (288) 288
prader-willi syndrome - psychology (286) 286
expression (284) 284
rehabilitation (276) 276
care and treatment (275) 275
angelman-syndrome (269) 269
chromosome mapping (257) 257
prevalence (257) 257
mutation (256) 256
physiological aspects (254) 254
chromosome 15 (246) 246
nutritional and metabolic diseases (238) 238
imprinting (236) 236
cell biology (235) 235
health aspects (235) 235
prader‐willi syndrome (232) 232
region (232) 232
chromosomes (229) 229
growth hormone (224) 224
karyotyping (224) 224
mental-retardation (223) 223
somatotropin (221) 221
chromosome aberrations (220) 220
alleles (217) 217
body-composition (217) 217
human growth hormone - therapeutic use (211) 211
angelman (209) 209
education, special (208) 208
pregnancy (208) 208
base sequence (207) 207
risk factors (205) 205
ghrelin (204) 204
molecular sequence data (202) 202
syndrome (200) 200
prader-willi syndrome - metabolism (198) 198
polymerase chain reaction (197) 197
brain (194) 194
intellectual disability - genetics (194) 194
prader-willi syndrome - pathology (194) 194
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (15) 15
Collection Dvlpm't (Acquisitions) - Vendor file (6) 6
Online Resources - Online (6) 6
Holland Bloorview Kids Rehabilitation - Stacks (5) 5
OISE - Periodical Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Gerstein Science - Periodical Stacks (2) 2
Robarts - Stacks (2) 2
Gerstein Science - Bindery (1) 1
Scarborough Hospital - General (1) 1
Scarborough Hospital - Online (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 (6394) 6394
Spanish (108) 108
Japanese (103) 103
French (95) 95
German (61) 61
Chinese (37) 37
Polish (31) 31
Italian (27) 27
Portuguese (23) 23
Korean (21) 21
Czech (11) 11
Dutch (9) 9
Russian (8) 8
Hungarian (7) 7
Turkish (7) 7
Danish (6) 6
Hebrew (3) 3
Norwegian (3) 3
Slovak (3) 3
Swedish (3) 3
Romanian (2) 2
Serbian (2) 2
Afrikaans (1) 1
Arabic (1) 1
Catalan (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Trends in Genetics, ISSN 0168-9525, 2017, Volume 33, Issue 8, pp. 540 - 552
Long noncoding RNAs (lncRNAs) are emerging as potential key regulators in gene expression networks and exhibit a surprising range of shapes and sizes. Several... 
Medical Education | MESSENGER-RNAS | CIRCRNA BIOGENESIS | CIRCULAR RNAS | PROMOTERS | TRANSCRIPTION | GENETICS & HEREDITY | GENE-EXPRESSION | TRIPLE-HELIX | XENOPUS-TROPICALIS | PRADER-WILLI-SYNDROME | EXON CIRCULARIZATION | Transcription, Genetic | RNA, Messenger - genetics | RNA, Long Noncoding - genetics | Ribonuclease | RNA | Gene expression | Genomics | Cells
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1995, Volume 4, Issue 5, pp. 801 - 806
Journal Article
Journal of Pediatric Nursing, ISSN 0882-5963, 09/2017, Volume 36, pp. 263 - 264
Journal Article
Revue Francophone des Laboratoires, ISSN 1773-035X, 04/2016, Volume 2016, Issue 481, p. 11
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 08/2005, Volume 6, Issue 8, pp. 597 - 610
Journal Article
Pediatric Obesity, ISSN 2047-6302, 01/2020, Volume 15, Issue 1, pp. e12575 - n/a
Summary Background Obesity control in Prader‐Willi syndrome (PWS) is notoriously difficult. The role of bariatric surgery in PWS remains controversial as... 
weight loss | bariatric surgery | morbid | obesity, paediatric obesity | Prader‐Willi syndrome
Journal Article
Journal Article
Enfermeria Clinica, ISSN 1130-8621, 11/2013, Volume 23, Issue 6, pp. 290 - 297
We report the case of a term infant of 39+1, born by emergency cesarean section due to suspected fetal distress with an Apgar test 4/6/8 and axial hypotonia... 
Apgar | Prader-Willi | Hypotonic
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2015, Volume 19, pp. S132 - S132
Objective Prader-Willi syndrome (PWS) is one of the more common causes of severe neonatal hypotonia. PWS is seen in 1:15000 newborn. The clinical picture is... 
Pediatrics | Neurology | Prader-Willi syndrome | Infants
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2013, Volume 368, Issue 26, pp. 2467 - 2475
Journal Article