X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (11423) 11423
Newspaper Article (3509) 3509
Publication (1723) 1723
Book / eBook (383) 383
Book Review (121) 121
Magazine Article (38) 38
Book Chapter (36) 36
Reference (11) 11
Dissertation (9) 9
Trade Publication Article (9) 9
Web Resource (9) 9
Conference Proceeding (8) 8
Data Set (8) 8
Government Document (2) 2
Report (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
urogenital system (9312) 9312
humans (7585) 7585
female (5199) 5199
male (4343) 4343
index medicus (4248) 4248
urine (3897) 3897
bladder (3892) 3892
infections (3662) 3662
antibiotics (3549) 3549
women (3505) 3505
bacteria (3330) 3330
bacterial infections (3296) 3296
excretory system (3207) 3207
berries (3165) 3165
research & development--r&d (3119) 3119
urogenital abnormalities (2529) 2529
animals (2149) 2149
adult (1780) 1780
pregnancy (1493) 1493
child (1351) 1351
endocrine system (1278) 1278
urology & nephrology (1224) 1224
urologic and male genital diseases (1214) 1214
infant, newborn (1200) 1200
pediatrics (1188) 1188
infant (1119) 1119
diagnosis (1028) 1028
mice (1022) 1022
child, preschool (1021) 1021
medicine (1020) 1020
adolescent (1017) 1017
research (1002) 1002
surgery (956) 956
middle aged (951) 951
urology (938) 938
article (927) 927
urinary tract infections (906) 906
uterus - abnormalities (815) 815
urinary tract diseases (811) 811
female genital diseases and pregnancy complications (793) 793
patients (785) 785
kidney - abnormalities (766) 766
research article (750) 750
health aspects (745) 745
risk factors (731) 731
kidneys (700) 700
medicine & public health (669) 669
analysis (660) 660
care and treatment (648) 648
children (645) 645
kidney diseases (633) 633
genetics & heredity (622) 622
retrospective studies (622) 622
obstetrics & gynecology (620) 620
urinary tract (617) 617
reproductive and urinary physiology (604) 604
aged (584) 584
mutation (573) 573
studies (566) 566
urogenital abnormalities - diagnosis (558) 558
treatment outcome (536) 536
cell biology (513) 513
developmental biology (507) 507
multidisciplinary sciences (506) 506
ultrasonography (481) 481
urogenital abnormalities - surgery (481) 481
diseases (473) 473
expression (457) 457
kidney (457) 457
infertility (452) 452
case report (449) 449
abnormalities (447) 447
disease (439) 439
proteins (439) 439
ultrasonic imaging (439) 439
syndrome (436) 436
cancer (428) 428
rodents (424) 424
science (415) 415
sperm (389) 389
young adult (389) 389
spermatozoa (388) 388
nephrology (381) 381
original (381) 381
gene expression (380) 380
genetic aspects (380) 380
physiological aspects (379) 379
congenital abnormalities (372) 372
oncology (372) 372
follow-up studies (361) 361
management (357) 357
biology (352) 352
embryonic structures (351) 351
urogenital abnormalities - complications (349) 349
review (346) 346
pathology (345) 345
age (344) 344
congenital, hereditary, and neonatal diseases and abnormalities (344) 344
gynecology (342) 342
urogenital abnormalities - genetics (341) 341
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (272) 272
Collection Dvlpm't (Acquisitions) - Vendor file (20) 20
Collection Dvlpm't (Acquisitions) - Closed Orders (18) 18
Scarborough Hospital - General (15) 15
Online Resources - Online (13) 13
St. Michael's Hospital - Stacks (9) 9
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (9) 9
Humber River Regional Hospital - Finch Stacks (6) 6
Lakeridge Health Sciences - Oshawa (6) 6
Holland Bloorview Kids Rehabilitation - Stacks (5) 5
Toronto East General Hospital - Stacks (5) 5
Robarts - Stacks (4) 4
Scarborough Hospital - Birchmount (4) 4
UofT at Mississauga - Stacks (4) 4
Credit Valley Hospital - Stacks (3) 3
Trillium Health Centre - Stacks (3) 3
Women's College Hospital - Stacks (3) 3
Credit Valley Hospital - Reference (2) 2
Humber River Regional Hospital - Church Stacks (2) 2
Law (Bora Laskin) - Stacks (2) 2
New College (Ivey) - Stacks (2) 2
Providence Healthcare - Reference (2) 2
Providence Healthcare - Stacks (2) 2
St Josephs Health Centre - Stacks (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
Trinity College (John W Graham) - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
Baycrest Hospital - Stacks (1) 1
Gerstein Science - Not Returned (1) 1
Gerstein Science - Reference (1) 1
Humber River Regional Hospital - Church Reference (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Mt Sinai Hospital - Online (1) 1
Providence Healthcare - Reserve desk (1) 1
Regis College - Stacks (1) 1
Royal Ontario Museum - Stacks (1) 1
Scarborough Hospital - Hospital Department (1) 1
St. Michael's Hospital - Circulation Desk (1) 1
Toronto East General Hospital - Online (1) 1
UofT at Mississauga - Oversize (1) 1
UofT at Mississauga - Reference (1) 1
UofT at Scarborough - Stacks (1) 1
West Park Healthcare Centre - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (14192) 14192
French (275) 275
German (257) 257
Italian (174) 174
Spanish (155) 155
Russian (90) 90
Polish (51) 51
Japanese (44) 44
Portuguese (43) 43
Chinese (37) 37
Dutch (26) 26
Czech (22) 22
Turkish (18) 18
Danish (13) 13
Hungarian (13) 13
Bulgarian (9) 9
Croatian (9) 9
Swedish (9) 9
Serbian (8) 8
Romanian (7) 7
Korean (6) 6
Arabic (5) 5
Hebrew (4) 4
Finnish (2) 2
Norwegian (2) 2
Slovak (2) 2
Slovenian (2) 2
Indonesian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2014, ISBN 0253012244, xiv, 261
"Putting the ethical tools of philosophy to work, Ellen K. Feder seeks to clarify how we should understand "the problem" of intersex. Adults often report that... 
Bioethics | Intersexuality | Moral and ethical aspects | Treatment
Book
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2014, Volume 211, Issue 6, pp. 675.e1 - 675.e19
Objective We sought to examine the association between increased first-trimester fetal nuchal translucency (NT) measurement and major noncardiac structural... 
Obstetrics and Gynecology | congenital birth defects | increased nuchal translucency | normal karyotype | prenatal screening | 1ST-TRIMESTER | GESTATION | CHROMOSOMALLY NORMAL FETUSES | PROGRAM | PREGNANCY | PATHOPHYSIOLOGY | OBSTETRICS & GYNECOLOGY | Urogenital Abnormalities - diagnostic imaging | Bone Diseases, Metabolic - epidemiology | Congenital Abnormalities - epidemiology | Intestine, Small - abnormalities | Musculoskeletal Abnormalities - epidemiology | Urogenital Abnormalities - epidemiology | Humans | Lung - abnormalities | Risk | Lung - diagnostic imaging | Nervous System Malformations - diagnostic imaging | Lung Diseases - diagnostic imaging | Young Adult | Hydrocephalus - diagnostic imaging | Abnormalities, Multiple - epidemiology | Hydrocephalus - epidemiology | Adult | Female | Intestinal Atresia - epidemiology | Diaphragm - abnormalities | Bone Diseases, Metabolic - diagnostic imaging | Musculoskeletal Abnormalities - diagnostic imaging | Abnormalities, Multiple - diagnostic imaging | Logistic Models | Congenital Abnormalities - diagnostic imaging | Nervous System Malformations - epidemiology | Pregnancy | Bone Diseases, Metabolic - congenital | Ultrasonography, Prenatal | Intestinal Atresia - diagnostic imaging | Nuchal Translucency Measurement | Adolescent | Intestine, Small - diagnostic imaging | Lung Diseases - epidemiology | Cohort Studies | Measurement | Infants | Birth defects | Public health
Journal Article
Journal Article
Genetics in Medicine, ISSN 1098-3600, 07/2018, Volume 20, Issue 7, pp. 745 - 753
Journal Article
Human Mutation, ISSN 1059-7794, 11/2012, Volume 33, Issue 11, pp. 1520 - 1525
Genitopatellar syndrome (GPS) and Say–Barber–Biesecker–Young–Simpson syndrome (SBBYSS or Ohdo syndrome) have both recently been shown to be caused by distinct... 
MYST4 | database | genitopatellar syndrome | KAT6B | Ohdo syndrome | Database | Genitopatellar syndrome | BLEPHAROPHIMOSIS | PROTEIN | MENTAL-RETARDATION | ANOMALIES | PHENOTYPE | ACUTE MYELOID-LEUKEMIA | HISTONE ACETYLTRANSFERASE | MORF | GENETICS & HEREDITY | OHDO-SYNDROME | QUERKOPF | Abnormalities, Multiple - pathology | Sequence Deletion | Scrotum - abnormalities | Kidney - pathology | Blepharoptosis - genetics | Histone Acetyltransferases - chemistry | Blepharophimosis - enzymology | Humans | Kidney - enzymology | Psychomotor Disorders - enzymology | Urogenital Abnormalities - enzymology | Histone Acetyltransferases - genetics | Molecular Sequence Data | Blepharophimosis - pathology | Male | Intellectual Disability - genetics | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Psychomotor Disorders - genetics | Base Sequence | Blepharoptosis - enzymology | Heart Defects, Congenital - enzymology | Patella - abnormalities | Intellectual Disability - enzymology | Craniofacial Abnormalities - pathology | Female | Scrotum - pathology | Patella - enzymology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Scrotum - enzymology | Genetic Association Studies | Heart Defects, Congenital - pathology | Intellectual Disability - pathology | Psychomotor Disorders - pathology | Haploinsufficiency | Patella - pathology | DNA - genetics | Urogenital Abnormalities - pathology | Kidney - abnormalities | Craniofacial Abnormalities - enzymology | Abnormalities, Multiple - enzymology | Mutation | Blepharoptosis - pathology | Databases, Nucleic Acid | Urogenital Abnormalities - genetics | Histones | Medical colleges | Congenital heart disease | Genetic disorders | Kidney diseases | Genes | Ohdo Syndrome | mutation database
Journal Article
Clinical Genetics, ISSN 0009-9163, 02/2017, Volume 91, Issue 2, pp. 339 - 343
Say–Barber–Biesecker–Young–Simpson syndrome (SBBYSS) and genitopatellar syndrome (GTPTS) are clinically similar disorders with some overlapping features.... 
Say–Barber–Biesecker–Young–Simpson syndrome, SBBYSS | KAT6B | lysine acetyltransferase 6B | genitopatellar syndrome | KAT6B spectrum disorders | GTPTS | KAT6B‐related disorders | KAT6B-related disorders | BLEPHAROPHIMOSIS | HISTONE ACETYLTRANSFERASE | FEATURES | RETARDATION | Say-Barber-Biesecker-Young-Simpson syndrome, SBBYSS | GENETICS & HEREDITY | MUTATIONS | SPECTRUM | Abnormalities, Multiple - pathology | Scrotum - abnormalities | Kidney - pathology | Exons | Humans | Joint Instability - genetics | Child, Preschool | Histone Acetyltransferases - genetics | Joint Instability - pathology | Blepharophimosis - pathology | Intellectual Disability - genetics | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Psychomotor Disorders - genetics | Congenital Hypothyroidism - diagnosis | Blepharophimosis - diagnosis | Congenital Hypothyroidism - genetics | Facies | Patella - abnormalities | Craniofacial Abnormalities - pathology | Female | Scrotum - pathology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Joint Instability - diagnosis | Urogenital Abnormalities - diagnosis | Heart Defects, Congenital - pathology | Intellectual Disability - pathology | Psychomotor Disorders - pathology | Patella - pathology | Phenotype | Urogenital Abnormalities - pathology | Craniofacial Abnormalities - diagnosis | Kidney - abnormalities | Abnormalities, Multiple - diagnosis | Intellectual Disability - diagnosis | Psychomotor Disorders - diagnosis | Congenital Hypothyroidism - pathology | Heart Defects, Congenital - diagnosis | Mutation | Urogenital Abnormalities - genetics | Genetic disorders | Multiprocessing | Lysine | Genetic aspects | Nucleotide sequencing | DNA sequencing | Genotype & phenotype
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2015, Volume 23, Issue 9, pp. 1165 - 1170
KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Biesecker type of blepharophimosis mental retardation syndromes... 
BLEPHAROPHIMOSIS | OHDO SYNDROME | DE-NOVO MUTATIONS | MENTAL-RETARDATION | HISTONE ACETYLTRANSFERASE KAT6B | CAUSE GENITOPATELLAR SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | Scrotum - abnormalities | Kidney - pathology | Exons | Humans | Joint Instability - genetics | Child, Preschool | Histone Acetyltransferases - genetics | Joint Instability - pathology | Blepharophimosis - pathology | Male | Intellectual Disability - genetics | Exome | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Psychomotor Disorders - genetics | Congenital Hypothyroidism - diagnosis | DNA Mutational Analysis | Blepharophimosis - diagnosis | Congenital Hypothyroidism - genetics | Facies | Patella - abnormalities | Craniofacial Abnormalities - pathology | Female | Scrotum - pathology | Craniofacial Abnormalities - genetics | Severity of Illness Index | Diagnosis, Differential | Gene Expression | Joint Instability - diagnosis | Genetic Association Studies | Urogenital Abnormalities - diagnosis | Heart Defects, Congenital - pathology | Intellectual Disability - pathology | Psychomotor Disorders - pathology | Genotype | Patella - pathology | Phenotype | Urogenital Abnormalities - pathology | Craniofacial Abnormalities - diagnosis | Kidney - abnormalities | Intellectual Disability - diagnosis | Psychomotor Disorders - diagnosis | Congenital Hypothyroidism - pathology | Heart Defects, Congenital - diagnosis | Mutation | Urogenital Abnormalities - genetics | Pediatrics | Phenotypes | Congenital diseases | Statistical analysis | Splicing | Intellectual disabilities | Thyroid gland | Blepharophimosis | Gene deletion | Defects | Haploinsufficiency | Medicine | Genotype & phenotype | Hospitals | Molecular modelling | Clonal deletion | Genetics | Genotypes | Thyroid | Life Sciences | Human genetics
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 12/2016, Volume 36, Issue 13, pp. 1270 - 1275
Journal Article
Journal Article
Journal Article