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

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (36) 36
life sciences & biomedicine (29) 29
humans (25) 25
genetics & heredity (19) 19
female (17) 17
male (17) 17
mutation (17) 17
genetic aspects (11) 11
genomics (11) 11
genes (10) 10
genetics (10) 10
developmental disabilities - genetics (9) 9
genomes (9) 9
research (9) 9
child (8) 8
adolescent (7) 7
biological and medical sciences (7) 7
multidisciplinary sciences (7) 7
science & technology - other topics (7) 7
biochemistry & molecular biology (6) 6
child, preschool (6) 6
chromosomes (6) 6
fundamental and applied biological sciences. psychology (6) 6
in situ hybridization, fluorescence (6) 6
adult (5) 5
analysis (5) 5
animals (5) 5
exome (5) 5
exome sequencing (5) 5
genetic variation (5) 5
genetics of eukaryotes. biological and molecular evolution (5) 5
medical genetics (5) 5
medical sciences (5) 5
neurodevelopmental disorders (5) 5
phenotype (5) 5
science (5) 5
translocation, genetic (5) 5
chromosome aberrations (4) 4
chromosome deletion (4) 4
cohort studies (4) 4
cytogenetics (4) 4
deoxyribonucleic acid--dna (4) 4
developmental disabilities (4) 4
disorders (4) 4
exome - genetics (4) 4
gene mutations (4) 4
genetic research (4) 4
infant, newborn (4) 4
methods (4) 4
mice (4) 4
mutation - genetics (4) 4
risk factors (4) 4
array-cgh (3) 3
cell line (3) 3
child development deviations (3) 3
chromosome mapping (3) 3
congenital diseases (3) 3
dna (3) 3
dna helicase (3) 3
dna microarrays (3) 3
gene sequencing (3) 3
general aspects. genetic counseling (3) 3
gtp-binding proteins - metabolism (3) 3
health aspects (3) 3
heredity (3) 3
histone-lysine n-methyltransferase - genetics (3) 3
human genetics (3) 3
identification and classification (3) 3
infant (3) 3
medical research (3) 3
middle aged (3) 3
molecular and cellular biology (3) 3
molecular sequence data (3) 3
oligonucleotide array sequence analysis (3) 3
pedigree (3) 3
polymorphism, single nucleotide (3) 3
proteins (3) 3
usage (3) 3
whole exome sequencing - methods (3) 3
abnormalities (2) 2
abnormalities, multiple - genetics (2) 2
abridged index medicus (2) 2
animal models (2) 2
author (2) 2
autoantigens (2) 2
autoantigens - genetics (2) 2
biomedical research (2) 2
biotechnology & applied microbiology (2) 2
cardiovascular diseases (2) 2
cdc2 protein kinase (2) 2
cdc2 protein kinase - genetics (2) 2
cdc42 gtp-binding protein (2) 2
cell cycle proteins - metabolism (2) 2
chromatin remodeling (2) 2
chromatin remodelling (2) 2
chromosomes, human, pair 6 - genetics (2) 2
classical genetics, quantitative genetics, hybrids (2) 2
clinical epigenetics (2) 2
comparative genomic hybridization - methods (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Lancet (British edition), ISSN 0140-6736, 2015, Volume 385, Issue 9975, pp. 1305 - 1314
Journal Article
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
Nature neuroscience, ISSN 1097-6256, 03/2016, Volume 19, Issue 4, pp. 571 - 577
Journal Article
by Sifrim, Alejandro and Hitz, Marc-Phillip and Wilsdon, Anna and Breckpot, Jeroen and Turki, Saeed H. Al and Thienpont, Bernard and McRae, Jeremy and Fitzgerald, Tomas W and Singh, Tarjinder and Swaminathan, Ganesh Jawahar and Prigmore, Elena and Rajan, Diana and Abdul-Khaliq, Hashim and Banka, Siddharth and Bauer, Ulrike M.M and Bentham, Jamie and Berger, Felix and Bhattacharya, Shoumo and Bu'Lock, Frances and Canham, Natalie and Colgiu, Irina-Gabriela and Cosgrove, Catherine and Cox, Helen and Daehnert, Ingo and Daly, Allan and Danesh, John and Fryer, Alan and Gewillig, Marc and Hobson, Emma and Hoff, Kirstin and Homfray, Tessa and Kahlert, Anne-Karin and Ketley, Ami and Kramer, Hans-Heiner and Lachlan, Katherine and Lampe, Anne Katrin and Louw, Jacoba J and Manickara, Ashok Kumar and Manase, Dorin and McCarthy, Karen P and Metcalfe, Kay and Moore, Carmel and Newbury-Ecob, Ruth and Omer, Seham Osman and Ouwehand, Willem H and Park, Soo-Mi and Parker, Michael J and Pickardt, Thomas and Pollard, Martin O and Robert, Leema and Roberts, David J and Sambrook, Jennifer and Setchfield, Kerry and Stiller, Brigitte and Thornborough, Chris and Toka, Okan and Watkins, Hugh and Williams, Denise and Wright, Michael and Mital, Seema and Daubeney, Piers E.F and Keavney, Bernard and Goodship, Judith and Abu-Sulaiman, Riyadh Mahdi and Klaassen, Sabine and Wright, Caroline F and Firth, Helen V and Barrett, Jeffrey C and Devriendt, Koenraad and Fitzpatrick, David R and Brook, J David and Hurles, Matthew E and INTERVAL Study and Deciphering Dev Disorders Study and UK10K Consortium and the INTERVAL Study and the Deciphering Developmental Disorders Study and the UK10K Consortium
Nature genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, pp. 1060 - 1065
Journal Article
Science (American Association for the Advancement of Science), ISSN 0036-8075, 12/2018, Volume 362, Issue 6419, pp. 1161 - 1164
Journal Article