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2016, Third edition., ISBN 1451176058, 944
eBook
2000, 2nd ed., ISBN 0192628267, xxii, 591
Book
European heart journal, ISSN 0195-668X, 10/2014, Volume 35, Issue 39, pp. 2733 - 2779
Heart failure | Hypertension | Valve disease | Arrhythmia | Left ventricular outflow tract obstruction | Sudden cardiac death | Athletes | Guidline | Pregnancy | Cardiac imaging | Genetics | Diagnosis | Symptoms | Implantable cardioverter defibrillators | Guideline | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Physical Examination - methods | Humans | Death, Sudden, Cardiac - prevention & control | Angina Pectoris - etiology | Genetic Testing - methods | Ventricular Outflow Obstruction - etiology | Sports Medicine | Adult | Female | Heart Valve Diseases - diagnosis | Cardiac Imaging Techniques - methods | Pregnancy Complications, Cardiovascular - diagnosis | Cardiomyopathy, Hypertrophic - etiology | Cardiomyopathy, Hypertrophic - therapy | Child | Heart Failure - etiology | Electrocardiography - methods | Pregnancy Complications, Cardiovascular - therapy | Diagnosis, Differential | Prenatal Care - methods | Risk Factors | Genetic Counseling - methods | Medical History Taking - methods | Arrhythmias, Cardiac - etiology | Cardiac Pacing, Artificial - methods | Cardiomyopathy, Hypertrophic - diagnosis | Clinical Laboratory Techniques - methods | Ablation Techniques - methods | Delivery of Health Care | Pedigree | Syncope - etiology | Heart Valve Diseases - therapy | Preconception Care - methods | Thoracic Surgical Procedures - methods | Index Medicus | Medicin och hälsovetenskap
Journal Article
2003, Issues in biomedical ethics, ISBN 9780199241323, xxvii, 554
Book
1999, ISBN 9780309062862, xiii, 397
Book
2006, STU - Student edition, In-formation series, ISBN 9780691121925, xxii, 256
Book
1998, Blackwell companions to philosophy., ISBN 0631197370, xv, 512
Book
The New England journal of medicine, ISSN 0028-4793, 12/2012, Volume 367, Issue 23, pp. 2175 - 2184
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Fetal Diseases - diagnosis | Oligonucleotide Array Sequence Analysis | Chromosomes, Human - genetics | Humans | Genetic Testing - methods | Pregnancy | Maternal Age | Ultrasonography, Prenatal | Karyotyping | Chromosome Aberrations | Chromosome Disorders - diagnosis | Adult | Female | Down Syndrome - diagnosis | Prenatal Diagnosis - methods | Karyotype | Usage | DNA microarrays | Prenatal diagnosis | Diagnosis | Research | Comparative analysis | Developmental delay | Health aspects | Methods | Fetuses | Genes | Tissue culture | Prenatal development | Genomes | Medical diagnosis | Autism | Chromosome translocations | Down's syndrome | Ultrasonography | Children | Triploidy | Chromosomes | Index Medicus | Abridged Index Medicus
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2012, Volume 20, Issue 1, pp. 27 - 32
pan-ethnic | carrier screening | SMN1 | spinal muscular atrophy (SMA) | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Neurology | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Muscular Atrophy, Spinal - diagnosis | United States - epidemiology | Humans | Male | Genetic Counseling | Genetic Testing - methods | Genetic Carrier Screening - methods | DNA Copy Number Variations | Muscular Atrophy, Spinal - genetics | Ethnic Groups - genetics | Survival of Motor Neuron 1 Protein - genetics | Adult | Female | Prenatal Diagnosis - statistics & numerical data | Reproducibility of Results | United States - ethnology | Genetic Testing - standards | Muscular Atrophy, Spinal - ethnology | Gene Frequency | Muscular Atrophy, Spinal - epidemiology | Genotype | Sequence Analysis, DNA | Fetus - cytology | Prenatal Diagnosis - standards | Mutation | Prenatal Diagnosis - methods | Laboratories | Families & family life | Cystic fibrosis | Family medical history | Minority & ethnic groups | Population genetics | Genetic screening | Hereditary diseases | Spinal muscular atrophy | Ethnicity | Prenatal diagnosis | Genetic counseling | Gene frequency | Alleles | Ethnic groups | Fibrosis | Population | Genetics | Quantitative analysis | Index Medicus
Journal Article