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informed consent (6) 6
moral and ethical aspects (6) 6
amino acid sequence (4) 4
bioinformatics (4) 4
citizen participation (4) 4
data processing (4) 4
dna (4) 4
genetics (4) 4
human experimentation in medicine (4) 4
medical ethics (4) 4
nucleotide sequence (4) 4
ethics (3) 3
computational biology [mesh] (2) 2
datenbank (2) 2
dna [mesh] (2) 2
dns (2) 2
ethics, medical [mesh] (2) 2
genetic research (2) 2
gesundheitswesen (2) 2
human experimentation (2) 2
humangenetik (2) 2
legislation & jurisprudence (2) 2
medical sociology (2) 2
new genetics (2) 2
philosophy & social aspects (2) 2
research subjects (2) 2
science (2) 2
social aspects (2) 2
sociology of health and illness (2) 2
sozialethik (2) 2
technology & engineering (2) 2
adaptation (1) 1
amino acid sequence analysis (1) 1
amino acid sequence databases (1) 1
amino acids (1) 1
analysis (1) 1
analysis, amino acid sequence (1) 1
analysis, nucleic acid sequence (1) 1
analysis, nucleotide sequence (1) 1
aspectos morais e éticos (1) 1
aspectos morales y éticos (1) 1
base sequence (1) 1
bases de datos (1) 1
bio-informatics (1) 1
bioethics (1) 1
bioinformatics. gene structure analysis. computer applications (1) 1
biological and medical sciences (1) 1
biological informatics (1) 1
biological specimen banks (1) 1
biology (1) 1
biomedical ethics (1) 1
biomedical research (1) 1
breeding (1) 1
cadenas de nucleótidos (1) 1
chromosomes (1) 1
clinical ethics (1) 1
clinical trials (1) 1
community participation (1) 1
computational biology (1) 1
consent (1) 1
consent to treatment (1) 1
consent, informed (1) 1
consentimento consciente (1) 1
consentimiento legal (1) 1
data banks (1) 1
data bases (1) 1
databanks (1) 1
database systems (1) 1
databases as topic (1) 1
databases citizen participation (1) 1
databases, genetic (1) 1
deoxyribonucleic acid (1) 1
deoxyribose (1) 1
desoxyribonucleic acid (1) 1
disclosure, medical (1) 1
dna data banks (1) 1
dna sequence (1) 1
electronic information resources (1) 1
embryology (1) 1
epidemiology (1) 1
ethics, medical (1) 1
experimentación humana en medicina (1) 1
genes (1) 1
genetic databases. moral and ethical aspects (1) 1
genetics data processing (1) 1
genetics, population (1) 1
genetics. social aspects. sociology (1) 1
genome databases. computer applications. molecular genetics (1) 1
genomics (1) 1
health behavior (1) 1
health care (1) 1
health care ethics (1) 1
health care sciences & services (1) 1
health participants (1) 1
health policy & services (1) 1
heredity (1) 1
human experimentation in medicine moral and ethical aspects (1) 1
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1. Genetic databases
: socio-ethical issues in the collection and use of DNA
by Corrigan, Oonagh, 1957 and Tutton, Richard, 1972
2004, ISBN 9780415316798, 211
Databases | Nucleotide sequence | DNA | Amino acid sequence | Genetics | Data processing | Citizen participation | Bioinformatics | Medical ethics | Sociology of Health and Illness | New Genetics | Medical Sociology
Book
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2. The limits of consent
: a socio-ethical approach to human subject research in medicine
by Corrigan, Oonagh, 1957
2009, ISBN 9780199231461, xii, 234
Human experimentation in medicine | Moral and ethical aspects | Informed consent (Medical law) | Epidemiology | Public Health | Medical research | Biomedical research | Vulnerable populations | Consent | Clinical trials | Individual autonomy | Informed consent | gEnetic research
Book
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3. Full Text Donating and exploiting DNA
: social and ethical aspects of public participation in genetic databases
by Corrigan, Oonagh, 1957 and Tutton, Richard, 1972 and MyiLibrary
2004, ISBN 9780415316798
Databases | Nucleotide sequence | DNA | Amino acid sequence | Genetics | Data processing | Citizen participation | Bioinformatics | Medical ethics
eBook
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4. Full Text Genetic Databases
: Socio-Ethical Issues in the Collection and Use of DNA
by Richard Tutton and Oonagh Corrigan
07/2004, ISBN 9780415316798, 224
Sociology of Health and Illness | New Genetics
eBook
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5. The limits of consent
: a socio-ethical approach to human subject research in medicine
by Corrigan, Oonagh, 1957
2009, ISBN 9780199231461
Informed Consent | Moral and ethical aspects | Informed consent (Medical law) | Research Subjects | legislation & jurisprudence | ethics | Human experimentation in medicine | Human Experimentation
Web Resource
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6. The limits of consent
: a socio-ethical approach to human subject research in medicine
by Corrigan, Oonagh, 1957
2009, ISBN 9780199231461
Moral and ethical aspects | Informed consent (Medical law) | Human experimentation in medicine
Web Resource
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7. The limits of consent
: a socio-ethical approach to human subject research in medicine
by Corrigan, Oonagh, 1957
2009, ISBN 9780199231461
Moral and ethical aspects | Informed consent (Medical law) | Human experimentation in medicine
Web Resource
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8. Full Text Trust in the health-care provider-patient relationship: A systematic mapping review of the evidence base
by Brennan, Nicola and Barnes, Rebecca and Calnan, Mike and Corrigan, Oonagh and Dieppe, Paul and Entwistle, Vikki
International journal for quality in health care, ISSN 1353-4505, 2013, Volume 25, Issue 6, pp. 682 - 688
Health care | Quality indicators | Mapping review | Professional-patient relations | Trust | Health Care Sciences & Services | Health Policy & Services | Life Sciences & Biomedicine | Science & Technology | Public health. Hygiene-occupational medicine | Public health. Hygiene | Biological and medical sciences | Miscellaneous | Health participants | Medical sciences | Trust - psychology | Physician-Patient Relations | Health Behavior | Humans | Quality of Health Care | Index Medicus
Journal Article
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9. Genetic databases
: socio-ethical issues in the collection and use of DNA
by Tutton, Richard, 1972 and Corrigan, Oonagh, 1957
2004, ISBN 9780415316798
Databases | Nucleotide sequence | DNA | Amino acid sequence | Genetics | Data processing | Citizen participation | Bioinformatics | Medical ethics
Web Resource
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10. Full Text MORALITY, RISK AND INFORMED CONSENT IN CLINICAL DRUG TRIALS
by Corrigan, Oonagh
2005, ISBN 1844720144
Book Chapter
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