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2015, First edition., Oxford handbooks, ISBN 9780199639748, xvii, 683 pages
Book
Nature (London), ISSN 0028-0836, 09/2015, Volume 526, Issue 7571, pp. 75 - 81
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Amino Acid Sequence | Genetics, Population | Genetic Predisposition to Disease | Genome-Wide Association Study | Physical Chromosome Mapping | Genomics | Humans | Molecular Sequence Data | Genotype | Mutation Rate | Sequence Analysis, DNA | Genome, Human - genetics | Haplotypes - genetics | Homozygote | Genetics, Medical | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Quantitative Trait Loci - genetics | Sequence Deletion - genetics | Genetic research | Observations | Genetic variation | Methods | Studies | Algorithms | Molecular structure | Population | Genomes | Mutation | Artificial chromosomes | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
The Journal of nutrition, ISSN 0022-3166, 08/2019, Volume 149, Issue 8, pp. 1460 - 1469
Family Characteristics | Humans | Child, Preschool | Female | Infant | Male | Child Development | Cognition | Micronutrients - blood | Mothers | Infant, Newborn | Cohort Studies | Transferrin | Poverty | Intelligence | Cognitive ability | Birth | Longitude | Children & youth | Micronutrients | Child development | Maternal & child health | Cognition & reasoning | Education | Reasoning | Nutrients | Children | Index Medicus | dietary intake | cognitive development | home environment | micronutrients | Original | diarrhea | illness
Journal Article
Nature (London), ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Index Medicus | 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
Annals of neurology, ISSN 0364-5134, 10/2015, Volume 78, Issue 4, pp. 630 - 648
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Huntington Disease - complications | Sleep Wake Disorders - metabolism | Humans | Middle Aged | Adult | Female | Huntington Disease - diagnosis | Male | Sleep Wake Disorders - diagnosis | Asymptomatic Diseases | Huntington Disease - metabolism | Sleep Wake Disorders - etiology | Metabolism | Insomnia | Laboratories | Index Medicus
Journal Article
2016, ISBN 9780231160957, xiv, 316 pages
Book
2018, ISBN 9780813175324, 255 pages
Book
The Lancet (British edition), ISSN 0140-6736, 2015, Volume 385, Issue 9975, pp. 1305 - 1314
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Humans | Child, Preschool | Incidental Findings | Infant | Male | Developmental Disabilities - genetics | Genome, Human - genetics | Information Dissemination | Specimen Handling | Phenotype | Adolescent | Female | Heterozygote | Genetic Variation - genetics | Genome-Wide Association Study - methods | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Medical research | Analysis | Genomics | Medicine, Experimental | Genetic research | Genomes | Nucleotide sequencing | DNA sequencing | Mutation | Medical diagnosis | Genes | Developmental disabilities | Index Medicus | Abridged Index Medicus
Journal Article