X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (516) 516
Paper (141) 141
Publication (139) 139
Newspaper Article (116) 116
Patent (31) 31
Report (31) 31
Book / eBook (28) 28
Book Review (20) 20
Dissertation (16) 16
Book Chapter (6) 6
Conference Proceeding (6) 6
Magazine Article (5) 5
Trade Publication Article (4) 4
Web Resource (3) 3
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (179) 179
experiment (161) 161
physics (155) 155
particle physics (141) 141
physics - high energy physics - experiment (133) 133
high energy physics - experiment (130) 130
female (120) 120
index medicus (119) 119
male (112) 112
genetics & heredity (105) 105
high energy physics (98) 98
cern lhc coll (88) 88
experimental results (88) 88
physics of elementary particles and fields (64) 64
scattering [p p] (60) 60
colliding beams [p p] (59) 59
phenomenology (59) 59
[ phys.hexp ] physics [physics]/high energy physics - experiment [hep-ex] (57) 57
mutation (57) 57
adult (55) 55
phenotype (49) 49
nuclear experiment (48) 48
research (45) 45
child, preschool (44) 44
8000 gev-cms (43) 43
infant, newborn (42) 42
child (41) 41
genetics (38) 38
infant (37) 37
pedigree (34) 34
physical sciences (34) 34
adolescent (32) 32
atlas (32) 32
fysik (32) 32
p p: scattering (32) 32
natural sciences (30) 30
naturvetenskap (30) 30
particle physics - experiment (30) 30
dna methylation (29) 29
p p: colliding beams (29) 29
13000 gev-cms (28) 28
subatomic physics (28) 28
subatomär fysik (28) 28
mutations (27) 27
diagnosis (26) 26
methylation (26) 26
[phys.hexp]physics [physics]/high energy physics - experiment [hep-ex] (25) 25
abnormalities, multiple - genetics (25) 25
biochemistry & molecular biology (25) 25
genetic aspects (25) 25
article (24) 24
genomic imprinting (24) 24
middle aged (24) 24
syndrome (24) 24
chemistry (21) 21
children (21) 21
health aspects (21) 21
data analysis method (20) 20
diabetes (20) 20
diabetes mellitus - genetics (20) 20
genes (20) 20
gene (19) 19
genetic disorders (19) 19
hadron-hadron scattering (19) 19
physics, particles & fields (19) 19
analysis (18) 18
medicine (18) 18
metallurgy (18) 18
risk factors (18) 18
物理学 (18) 18
astrophysics (17) 17
background (17) 17
endocrinology & metabolism (17) 17
gene mutations (17) 17
high energy astrophysical phenomena (17) 17
journal article (17) 17
physik (17) 17
base sequence (16) 16
beckwith-wiedemann syndrome (16) 16
beckwith-wiedemann syndrome - genetics (16) 16
cinematography (16) 16
growth disorders - genetics (16) 16
molecular sequence data (16) 16
organic chemistry (16) 16
pediatrics (16) 16
peptides (16) 16
physiological aspects (16) 16
apparatus specially adapted therefor (15) 15
electrography (15) 15
engineering (15) 15
holography (15) 15
human necessities (15) 15
hygiene (15) 15
mass dependence (15) 15
materials therefor (15) 15
medical or veterinary science (15) 15
medical research (15) 15
mellitus (15) 15
mosaicism (15) 15
originals therefor (15) 15
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (8) 8
Gerstein Science - Stacks (5) 5
Online Resources - Online (5) 5
UofT at Mississauga - Stacks (3) 3
Victoria University E.J. Pratt - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
OISE - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
Chemistry (A D Allen) - Theses (1) 1
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Theses (1) 1
Innis College - Reference (1) 1
Innis College - Stacks (1) 1
Media Commons - Microtexts (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Trinity College (John W Graham) - Stacks (1) 1
University College (Laidlaw) - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Genetics, ISSN 0340-6717, 06/2014, Volume 133, Issue 6, p. 813
Journal Article
by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
Nature Reviews Endocrinology, ISSN 1759-5029, 02/2017, Volume 13, Issue 2, pp. 105 - 124
Journal Article
Drug and Therapeutics Bulletin, ISSN 0007-0769, 01/1981, Volume 45, Issue 1, p. 2
Impetigo is a superficial, but contagious, bacterial infection of the skin that predominantly affects children and is common in primary care. In UK general... 
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2017, Volume 100, Issue 5, pp. 725 - 736
Journal Article
Journal Article
Journal Article