Articles

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

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (64680) 64680
Book Chapter (2051) 2051
Newspaper Article (1668) 1668
Newsletter (553) 553
Book / eBook (420) 420
Magazine Article (108) 108
Dissertation (98) 98
Web Resource (55) 55
Conference Proceeding (35) 35
Book Review (25) 25
Journal / eJournal (20) 20
Streaming Video (19) 19
Publication (17) 17
Trade Publication Article (15) 15
Reference (13) 13
Report (11) 11
Government Document (10) 10
Paper (6) 6
Video Recording (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (48624) 48624
science & technology (39314) 39314
life sciences & biomedicine (38307) 38307
female (32761) 32761
male (25758) 25758
infant, newborn (15441) 15441
biological and medical sciences (15407) 15407
medical sciences (15050) 15050
adult (12930) 12930
infant (12497) 12497
pregnancy (11924) 11924
pediatrics (11827) 11827
child (11343) 11343
child, preschool (9871) 9871
genetic disorders (8667) 8667
congenital heart disease (8584) 8584
adolescent (8444) 8444
surgery (8303) 8303
congenital diseases (7712) 7712
abridged index medicus (7112) 7112
cardiovascular system & cardiology (7076) 7076
genetics & heredity (6969) 6969
cardiac & cardiovascular systems (6967) 6967
heart (6125) 6125
retrospective studies (5815) 5815
risk factors (5134) 5134
middle aged (4437) 4437
syndrome (4175) 4175
treatment outcome (4151) 4151
research (4062) 4062
diagnosis (4059) 4059
obstetrics & gynecology (4042) 4042
animals (4022) 4022
mutation (3997) 3997
medicine & public health (3961) 3961
health aspects (3503) 3503
follow-up studies (3490) 3490
cardiology. vascular system (3375) 3375
care and treatment (3290) 3290
birth defects (3208) 3208
magnetic resonance imaging (3184) 3184
heart defects, congenital - surgery (3183) 3183
medical genetics (3168) 3168
young adult (3070) 3070
prenatal diagnosis (3046) 3046
analysis (3037) 3037
children (3034) 3034
patients (2995) 2995
infants (2944) 2944
congenital defects (2937) 2937
radiology, nuclear medicine & medical imaging (2925) 2925
congenital anomalies (2920) 2920
echocardiography (2849) 2849
radiography (2829) 2829
heart diseases (2809) 2809
diagnosis, differential (2798) 2798
medicine (2724) 2724
heart defects, congenital - diagnosis (2717) 2717
abnormalities, multiple - genetics (2700) 2700
phenotype (2659) 2659
congenital heart diseases. malformations of the aorta, pulmonary vessels and vena cava (2483) 2483
congenital abnormalities (2481) 2481
cardiology (2433) 2433
ultrasonography, prenatal (2397) 2397
congenital, hereditary, and neonatal diseases and abnormalities (2390) 2390
heart defects, congenital - diagnostic imaging (2360) 2360
cardiovascular disease (2357) 2357
gestational age (2353) 2353
congenital abnormalities - epidemiology (2330) 2330
case report (2309) 2309
diseases of the osteoarticular system (2286) 2286
genetics (2283) 2283
tomography, x-ray computed (2278) 2278
gynecology. andrology. obstetrics (2272) 2272
congenital (2264) 2264
genetic aspects (2239) 2239
heart defects, congenital - complications (2236) 2236
pedigree (2128) 2128
malformations and congenital and or hereditary diseases involving bones. joint deformations (2086) 2086
heart defects, congenital - genetics (2057) 2057
mortality (1922) 1922
prognosis (1869) 1869
age (1834) 1834
aged (1817) 1817
electrocardiography (1806) 1806
ultrasonography (1806) 1806
prevalence (1780) 1780
pregnant women (1776) 1776
fetuses (1733) 1733
abnormalities (1730) 1730
respiratory system (1716) 1716
research article (1715) 1715
general & internal medicine (1694) 1694
neurosciences & neurology (1687) 1687
defects (1685) 1685
genes (1681) 1681
medical research (1656) 1656
ophthalmology (1603) 1603
usage (1597) 1597
time factors (1577) 1577
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (182) 182
Robarts - Stacks (37) 37
Collection Dvlpm't (Acquisitions) - Vendor file (36) 36
Online Resources - Online (27) 27
UofT at Mississauga - Stacks (22) 22
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (14) 14
Holland Bloorview Kids Rehabilitation - Stacks (13) 13
Collection Dvlpm't (Acquisitions) - Closed Orders (10) 10
UTL at Downsview - May be requested (10) 10
St. Michael's College (John M. Kelly) - 2nd Floor (9) 9
UofT at Scarborough - Stacks (9) 9
St. Michael's Hospital - Stacks (8) 8
Victoria University E.J. Pratt - Stacks (7) 7
New College (Ivey) - Stacks (5) 5
Lakeridge Health Sciences - Oshawa (4) 4
Scarborough Hospital - Online (4) 4
Thomas Fisher Rare Book - Rare Book (4) 4
Toronto East General Hospital - Stacks (4) 4
Credit Valley Hospital - Reserve desk (3) 3
Humber River Regional Hospital - Finch Stacks (3) 3
Law (Bora Laskin) - Stacks (3) 3
OISE - Stacks (3) 3
Scarborough Hospital - General (3) 3
Sunnybrook Health Sciences Centre - Online (3) 3
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (2) 2
Dentistry (Harry R Abbott) - Stacks (2) 2
Gerstein Science - Circulation Desk (2) 2
Holland Bloorview Kids Rehabilitation - Reference (2) 2
Mt Sinai Hospital - Pathology (2) 2
Pontifical Inst. Mediaeval Studies - Library use only (2) 2
St. Augustine's Seminary - Stacks (2) 2
St. Michael's College (John M. Kelly) - 3rd Floor (2) 2
St. Michael's Hospital - Circulation Desk (2) 2
Victoria University CRRS - Library use only (2) 2
Baycrest Hospital - Resident/Client Library (1) 1
Credit Valley Hospital - Missing (1) 1
Credit Valley Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Gerstein Science - Missing (1) 1
Gerstein Science - Reference (1) 1
Knox College (Caven) - Stacks (1) 1
Lakeridge Health Sciences - Online (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Media Commons - Audio Visual (1) 1
Mt Sinai Hospital - Stacks (1) 1
OISE - Children's Literature (1) 1
OISE - Missing (1) 1
Providence Healthcare - Stacks (1) 1
Regis College - Stacks (1) 1
Royal Ontario Museum - Periodical Stacks (1) 1
Royal Ontario Museum - Stacks (1) 1
Scarborough Hospital - Birchmount (1) 1
St Josephs Health Centre - Stacks (1) 1
Trillium Health Centre - Reserve desk (1) 1
Trinity College (John W Graham) - Stacks (1) 1
University College (Laidlaw) - Stacks (1) 1
UofT at Mississauga - Course Reserves (1) 1
UofT at Scarborough - May be requested in 6-10 wks (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
Victoria University E.J. Pratt - Rare Book (1) 1
Victoria University Emmanuel College - Stacks (1) 1
Women's College Hospital - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (65546) 65546
French (998) 998
German (991) 991
Spanish (904) 904
Japanese (739) 739
Portuguese (533) 533
Russian (277) 277
Polish (260) 260
Italian (245) 245
Korean (139) 139
Turkish (135) 135
Chinese (108) 108
Czech (88) 88
Bulgarian (60) 60
Hungarian (58) 58
Dutch (53) 53
Croatian (49) 49
Serbian (34) 34
Persian (22) 22
Slovak (22) 22
Romanian (21) 21
Hebrew (20) 20
Swedish (15) 15
Danish (13) 13
Norwegian (13) 13
Ukrainian (10) 10
Bosnian (6) 6
Finnish (6) 6
Slovenian (5) 5
Lithuanian (4) 4
Arabic (3) 3
Latvian (3) 3
Icelandic (2) 2
Bengali (1) 1
Estonian (1) 1
Greek (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Congenital anomalies
Nihon Senten Ijō Gakkai
Congenital anomalies, ISSN 1741-4520, 1987
Periodicals | Abnormalities, Human | Genetic disorders | Medical genetics
Journal
Details down arrow
2. Full Text Maternal Overweight and Obesity and the Risk of Congenital Anomalies: A Systematic Review and Meta-analysis
by Stothard, Katherine J and Tennant, Peter W. G and Bell, Ruth and Rankin, Judith
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 02/2009, Volume 301, Issue 6, pp. 636 - 650
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Obesity | Biological and medical sciences | Metabolic diseases | General aspects | Medical sciences | Pregnancy | Congenital Abnormalities - epidemiology | Overweight - complications | Obesity - complications | Humans | Pregnancy Complications | Risk Factors | Congenital Abnormalities - etiology | Female | Physiological aspects | Birth defects | Pregnant women | Risk factors | Mothers | Weight control | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN‐related epilepsy
by Fleming, Leah and Lemmon, Monica and Beck, Natalie and Johnson, Maria and Mu, Weiyi and Murdock, David and Bodurtha, Joann and Hoover‐Fong, Julie and Cohn, Ronald and Bosemani, Thangamadhan and Barañano, Kristin and Hamosh, Ada
American journal of medical genetics. Part A, ISSN 1552-4825, 01/2016, Volume 170, Issue 1, pp. 77 - 86
epilepsy | spasms | GPI ethanolamine phosphate transferase 1 | genotype‐phenotype association | infantile | PIGN | glycosylphosphatidylinositol anchors | intractable | human | hypotonia | congenital disorders of glycosylation | Human | Glycosylphosphatidylinositol anchors | Hypotonia | Intractable | Epilepsy | Infantile | Congenital disorders of glycosylation | Genotype-phenotype association | Spasms | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Prognosis | Seizures - genetics | Humans | Child, Preschool | Epilepsy - congenital | Infant | Male | Developmental Disabilities - genetics | Seizures - congenital | Young Adult | Developmental Disabilities - pathology | Seizures - pathology | Adult | Epilepsy - genetics | Female | Child | Phosphotransferases - genetics | Abnormalities, Multiple - genetics | Muscle Hypotonia - genetics | Genetic Association Studies | Genotype | Mutation - genetics | Syndrome | Muscle Hypotonia - congenital | Muscle Hypotonia - pathology | Phenotype | Pedigree | Adolescent | Epilepsy - pathology | Gastroesophageal reflux | Genetic aspects | Genetic disorders | Seizures (Medicine) | Index Medicus | genotype-phenotype association
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Airway Anomalies
by Landry, April M and Rutter, Michael J
Clinics in perinatology, ISSN 0095-5108, 12/2018, Volume 45, Issue 4, pp. 597 - 607
Airway anomalies | Glottic web | Complete tracheal rings | Laryngeal atresia | Congenital subglottic stenosis | Laryngeal cleft | Pediatrics | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Respiratory System Abnormalities - surgery | Congenital Abnormalities - epidemiology | Laryngoscopy - methods | Prevalence | Prognosis | Laryngostenosis - epidemiology | Tracheal Stenosis - surgery | Humans | Bronchoscopy - methods | Male | Congenital Abnormalities - diagnosis | Tracheal Stenosis - congenital | Female | Larynx - surgery | Respiratory System Abnormalities - diagnosis | Infant, Newborn | Risk Assessment | Tracheal Stenosis - diagnosis | Reconstructive Surgical Procedures - methods | Treatment Outcome | Larynx - abnormalities | Laryngostenosis - diagnosis | Respiratory System Abnormalities - epidemiology | Congenital Abnormalities - surgery | Tracheal Stenosis - epidemiology | Laryngostenosis - surgery
Journal Article
Details down arrow
5. Full Text Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
by Lord, Jenny and McMullan, Dominic J and Eberhardt, Ruth Y and Rinck, Gabriele and Hamilton, Susan J and Quinlan-Jones, Elizabeth and Prigmore, Elena and Keelagher, Rebecca and Best, Sunayna K and Carey, Georgina K and Mellis, Rhiannon and Robart, Sarah and Berry, Ian R and Chandler, Kate E and Cilliers, Deirdre and Cresswell, Lara and Edwards, Sandra L and Gardiner, Carol and Henderson, Alex and Holden, Simon T and Homfray, Tessa and Lester, Tracy and Lewis, Rebecca A and Newbury-Ecob, Ruth and Prescott, Katrina and Quarrell, Oliver W and Ramsden, Simon C and Roberts, Eileen and Tapon, Dagmar and Tooley, Madeleine J and Vasudevan, Pradeep C and Weber, Astrid P and Wellesley, Diana G and Westwood, Paul and White, Helen and Parker, Michael and Williams, Denise and Jenkins, Lucy and Scott, Richard H and Kilby, Mark D and Chitty, Lyn S and Hurles, Matthew E and Maher, Eamonn R and Bateman, Mark and Berry, Ian R and Best, Sunayna K and Campbell, Carolyn and Campbell, Jenni and Carey, Georgina and Chandler, Kate E and Chitty, Lyn S and Cilliers, Deirdre and Cohen, Kelly and Collingwood, Emma and Constantinou, Panayiotis and Cresswell, Lara and Delmege, Catherine and Eberhardt, Ruth Y and Edwards, Sandra L and Ellis, Richard and Evans, Jerry and Everett, Thomas and Pinto, Clare F and Forrester, Natalie and Fowler, Emma and Gardiner, Carol and Hamilton, Susan and Healey, Karen and Henderson, Alex and Holden, Simon T and Homfray, Tessa and Hudson, Rebecca and Hurles, Matthew E and Jenkins, Lucy and Keelagher, Rebecca and Kilby, Mark D and Lester, Tracey and Lewis, Rebecca and Lord, Jenny and Maher, Eamonn R and Marton, Tamas and McMullan, Dominic J and Mehta, Sarju and Mellis, Rhiannon and Newbury-Ecob, Ruth and Park, Soo-Mi and Parker, Michael and Prescott, Katrina and Prigmore, Elena and Quarrell, Oliver W and Quinlan-Jones, Elizabeth and Ramsden, Simon C and Rinck, Gabriele and Robart, Sarah and Roberts, Eileen and Rowland, Jayne and Scott, Richard H and Steer, James and Tapon, Dagmar and Taylor, Emma J and ... and Prenatal Assessment of Genomes and Exomes Consortium and Prenatal Assessment Genomes Exomes
The Lancet (British edition), ISSN 0140-6736, 02/2019, Volume 393, Issue 10173, pp. 747 - 757
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Fetus - abnormalities | Congenital Abnormalities - epidemiology | Fetus - diagnostic imaging | Prospective Studies | Humans | Parents | Perinatal Death - etiology | Male | DNA Copy Number Variations - genetics | Whole Exome Sequencing - methods | Abnormal Karyotype - embryology | Congenital Abnormalities - diagnosis | Pregnancy | Abortion, Spontaneous - epidemiology | Congenital Abnormalities - genetics | Nuchal Translucency Measurement | Stillbirth - epidemiology | Abnormal Karyotype - statistics & numerical data | Female | Live Birth - epidemiology | Fetal Development - genetics | Abortion, Eugenic - statistics & numerical data | Infant, Newborn | Whole Exome Sequencing - statistics & numerical data | Ultrasound imaging | Pregnant women | Heart | Intellectual disabilities | Copy number | Genes | Disorders | Prenatal development | Aneuploidy | Genomes | Gestation | Microcephaly | Genetic screening | Gene sequencing | Disability | Proteins | Parents & parenting | Ultrasonic imaging | Next-generation sequencing | Scoliosis | Heart diseases | Ultrasound | Deoxyribonucleic acid--DNA | Phenotypes | Congenital diseases | Research & development--R&D | Fetuses | Abnormalities | Birth defects | Heredity | Hearing impairment | Coronary artery disease | Genetic variance | DNA microarrays | Gene frequency | Diagnostic systems | Cardiovascular diseases | Anomalies | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Accuracy of Ultrasonography at 11–14 Weeks of Gestation for Detection of Fetal Structural Anomalies: A Systematic Review
by Rossi, A Cristina and Prefumo, Federico
Obstetrics and gynecology (New York. 1953), ISSN 0029-7844, 12/2013, Volume 122, Issue 6, pp. 1160 - 1167
Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Pregnancy | Ultrasonography, Prenatal | Humans | Female | Congenital Abnormalities - diagnostic imaging | Gestational Age | Pregnancy Trimester, First | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text An Approach to the Identification of Anomalies and Etiologies in Neonates with Identified or Suspected VACTERL (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula with Esophageal Atresia, Cardiac Anomalies, Renal Anomalies, and Limb Anomalies) Association
by Solomon, Benjamin D., MD and Baker, Linda A., MD and Bear, Kelly A., DO and Cunningham, Bridget K., MD and Giampietro, Philip F., MD, PhD and Hadigan, Colleen, MD and Hadley, Donald W., MS, CGC and Harrison, Steven, BS and Levitt, Marc A., MD and Niforatos, Nickie, MD and Paul, Scott M., MD and Raggio, Cathleen, MD and Reutter, Heiko, MD and Warren-Mora, Nicole, MD
The Journal of pediatrics, ISSN 0022-3476, 2014, Volume 164, Issue 3, pp. 451 - 457.e1
Pediatrics | Life Sciences & Biomedicine | Science & Technology | Limb Deformities, Congenital - genetics | Genetic Testing | Kidney - pathology | Humans | Esophagus - abnormalities | Blood Cell Count | Anal Canal - abnormalities | Spine - abnormalities | Trachea - pathology | Diagnostic Imaging | Heart Defects, Congenital - genetics | Limb Deformities, Congenital - diagnosis | Esophagus - pathology | Algorithms | Kidney - abnormalities | Electrocardiography | Physical Examination | Heart Defects, Congenital - diagnosis | Spine - pathology | Anal Canal - pathology | Infant, Newborn | Trachea - abnormalities | Infants (Newborn) | Genomics | Medical genetics | Index Medicus | Abridged Index Medicus | VACTERL | VATER association | VATER | VACTERL association
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Associated anomalies in cases with anorectal anomalies
by Stoll, Claude and Dott, Beatrice and Alembik, Yves and Roth, Marie‐Paule
American journal of medical genetics. Part A, ISSN 1552-4825, 12/2018, Volume 176, Issue 12, pp. 2646 - 2660
anorectal malformations | vertebral defects, anal atresia, cardiac septal defects, esophageal atresia or tracheoesophageal fistula, renal anomalies and radial limb defects | multiple congenital anomalies | anal anomalies | urogenital anomalies | anorectal anomalies | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Pregnancy | Vertebrae | Etiology | Congenital defects | Hernias | Fistulae | Anorectal | Sudden infant death syndrome--SIDS | Defects | Esophagus | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights