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2004, 1st Carroll & Graf ed., ISBN 9780786714988, xv, 319
Book
1891, 50
Book
1955, Protoplasmatologia : Handbuch der Protoplasmaforschung, Volume Bd. 2, T. b 2C., 172
Book
1996, ISBN 9780687011346, 392
Book
Global Plants Initiative Field Notes Collections.
Book
Global Plants Initiative Field Notes Collections.
Book
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 329 - 332
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Liver. Biliary tract. Portal circulation. Exocrine pancreas | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | B7-1 Antigen - genetics | Humans | Immunity, Innate - genetics | Databases, Genetic | Male | NF-kappa B p50 Subunit - genetics | Death Domain Receptor Signaling Adaptor Proteins - genetics | Lectins, C-Type - genetics | Case-Control Studies | Adaptive Immunity - genetics | Receptors, Interleukin-7 - genetics | Liver Cirrhosis, Biliary - immunology | Female | Monosaccharide Transport Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Guanine Nucleotide Exchange Factors - genetics | Receptors, CXCR5 - genetics | Risk Factors | Liver Cirrhosis, Biliary - genetics | Receptors, Tumor Necrosis Factor, Type I - genetics | Linkage Disequilibrium | STAT4 Transcription Factor - genetics | Polymorphism, Single Nucleotide | Cohort Studies | Care and treatment | Disease susceptibility | Genetic aspects | Biliary cirrhosis | Single nucleotide polymorphisms | Research | Risk factors | Medical research | Biomedical research | Disease | Health services | Genes | Genomes | Liver cirrhosis | Index Medicus | Medicin och hälsovetenskap
Journal Article
American journal of human genetics, ISSN 0002-9297, 04/2014, Volume 94, Issue 4, pp. 618 - 624
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Chromosome Deletion | Chromosomes, Human, Pair 3 | Humans | Adolescent | Methyltransferases - genetics | Male | Mutation | Child | Intellectual Disability - genetics | Psychological aspects | Gene mutations | Methyltransferases | Causes of | Genetic aspects | Chromosome deletion | Health aspects | Mental retardation | Genotype & phenotype | Learning disabilities | Behavior disorders | Genes | Index Medicus | Report
Journal Article
1994, ISBN 0195067703, xxiii, 272
Book
Human mutation, ISSN 1059-7794, 12/2015, Volume 36, Issue 12, pp. 1197 - 1204
developmental delay | Mendelian disease | intellectual disability | next‐generation sequencing | Intellectual disability | Next-generation sequencing | Developmental delay | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Inheritance Patterns | Computational Biology - methods | Genetic Association Studies | Humans | Alleles | Female | Male | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Mutation | Cohort Studies | Intellectual Disability - genetics | Parenting | Genetic disorders | Analysis | Cytogenetics | Family | Single nucleotide polymorphisms | Mental illness | Intellectual disabilities | Index Medicus | Life Sciences | Genetics | Human genetics | s
Journal Article
Nature communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, pp. 6124 - 6124
Journal Article
American journal of human genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 295 - 302
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Middle Aged | Child, Preschool | Male | Exome | Young Adult | Adult | Female | Child | Introns | Codon, Nonsense | Phosphoproteins - genetics | Eye Abnormalities - genetics | Phenotype | Animals | Eye Abnormalities - pathology | Pedigree | Transcription Initiation Site | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Alleles | Heterozygote | Nonsense Mediated mRNA Decay - genetics | Aged | Mice | Transcription Factors | Cell Cycle Proteins | Optic nerve | Gene mutations | Physiological aspects | Genetic research | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Genotype & phenotype | Mutation | Hybridization | Rodents | Index Medicus | Report
Journal Article
Cortex, ISSN 0010-9452, 01/2016, Volume 74, pp. 449 - 475
Gulf War illness | Cyclosarin | Pesticide | Veterans' health | Sarin | Organophosphates | Psychology, Experimental | Neurosciences | Social Sciences | Life Sciences & Biomedicine | Behavioral Sciences | Psychology | Neurosciences & Neurology | Science & Technology | Brain Neoplasms - chemically induced | Gulf War | Neurotoxins - poisoning | Occupational Exposure - adverse effects | Veterans | Cognition Disorders - chemically induced | Humans | Persian Gulf Syndrome - chemically induced | Fatigue - chemically induced | Index Medicus | Veterans’ health
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