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Volumn 10, Issue 3, 2015, Pages 334-337

Data Rights and Responsibilities: A Human Rights Perspective on Data Sharing

Author keywords

Article 15; data; ethics; human rights; informed consent; privacy; right to science

Indexed keywords

COOPERATION; ETHICS; HUMAN; HUMAN RIGHTS; INFORMATION DISSEMINATION; INFORMATION PROCESSING; INTERNATIONAL COOPERATION; MEDICAL RESEARCH; POLICY; SCIENCE; SOCIAL BEHAVIOR; SOCIAL NORM; SOCIAL PSYCHOLOGY;

EID: 84955253341     PISSN: 15562646     EISSN: 15562654     Source Type: Journal    
DOI: 10.1177/1556264615591558     Document Type: Review
Times cited : (8)

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    • Duke, C.S.1    Porter, J.H.2
  • 6
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    • A human rights approach to an international code of conduct for genomic and clinical data sharing
    • Knoppers B. M., Harris J. R., Budin-Ljøsne I., Dove E. S., (2014). A human rights approach to an international code of conduct for genomic and clinical data sharing. Human Genetics, 133, 895-903.
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    • Knoppers, B.M.1    Harris, J.R.2    Budin-Ljøsne, I.3    Dove, E.S.4
  • 7
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    • Core rights and obligations
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    • United Nations Educational, Science and Cultural Organization
    • United Nations Educational, Science and Cultural Organization. (2005). Universal declaration on Bioethics and Human Rights. Retrieved from http://www.unesco.org/new/en/social-and-human-sciences/themes/bioethics/bioethics-and-human-rights/
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.