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2005, ISBN 0789018713, xxvi, 321
Book
2012, ISBN 0691156042, xiii, 809 p., [16] p. of plates
Book
1966, Politics of modernization series, Volume no. 1, 129
Book
Science (American Association for the Advancement of Science), ISSN 0036-8075, 07/2018, Volume 361, Issue 6398, p. eaat1378
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Sky | Red shift | Atmospheric models | Gravitational waves | Luminosity | Emission | Activation | Supernova 1987A | Cosmic radiation | Cosmic rays | Energy | Radio sources (astronomy) | Cooperation | Neutrinos | Gravity | Fluctuations | Statistical analysis | Electromagnetic radiation | Blazars | Universe | Photons | Line of sight | Relativistic effects | Emissions | Gamma rays | Observatories | X rays | Wavelengths | Spatial distribution | Collaboration | Telescopes | Relativism | Acceleration | Astronomy | Tracers | Atomic, Nuclear and Particle Physics | ASTRONOMY AND ASTROPHYSICS
Journal Article
2009, ISBN 9780674033276, x, 302
Book
Nature (London), ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 68 - 74
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Rare Diseases - genetics | Genome-Wide Association Study | Datasets as Topic | Demography | Disease Susceptibility | Physical Chromosome Mapping | Humans | Genetics, Population - standards | Genomics - standards | Genotype | INDEL Mutation - genetics | Sequence Analysis, DNA | Genome, Human - genetics | Haplotypes - genetics | Exome - genetics | Reference Standards | Genetics, Medical | Internationality | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | High-Throughput Nucleotide Sequencing | Quantitative Trait Loci - genetics | Genetic research | Nucleotide sequencing | Observations | Genetic variation | Methods | DNA sequencing | Studies | Haplotypes | Genotype & phenotype | Accuracy | Genealogy | Population | Genomes | Genetic diversity | Mitochondrial DNA | Binding sites | Index Medicus
Journal Article
American journal of human genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 233 - 245
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Dyslipidemias - genetics | Genetic Code | Follow-Up Studies | Humans | Middle Aged | Male | Proprotein Convertases - genetics | Exome | Dyslipidemias - blood | Serine Endopeptidases - genetics | Adult | Female | Receptors, LDL - genetics | Genome-Wide Association Study | Gene Frequency | Genotype | Sequence Analysis, DNA | Cholesterol, LDL - genetics | Phenotype | Apolipoproteins E - blood | Apolipoproteins E - genetics | Aged | Polymorphism, Single Nucleotide | Cohort Studies | Lipase - genetics | Proprotein Convertase 9 | Genetic code | Genetic variation | Physiological aspects | Genetic research | Cholesterol, LDL | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Genotype & phenotype | Low density lipoprotein | Genes | Cholesterol | Risk factors | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article