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Health Policy (Amsterdam, Netherlands)|March 24, 2007
Patient rights in EU Member States after the ratification of the Convention on Human Rights and BiomedicineHerman Nys, Loes Stultiëns, Pascal Borry, et al.
Accountability in Research|November 30, 2022
Assessing the acceptability of individual studies that use deception: A systematic review of normative guidance documentsKamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2021
Disclosure of genetic information to family members: a systematic review of normative documentsAmicia Phillips, Pascal Borry, Ine Van Hoyweghen, et al.
European Journal of Human Genetics : EJHG|March 9, 2017
Paternity testing under the cloak of recreational geneticsNathalie Moray, Katherina E Pink, Pascal Borry, et al.
Accountability in Research|June 3, 2024
Truthfulness as the basis for ethical safeguards in deceptive research: An interview study with researchersKamiel Verbeke, Jan Piasecki, Dieter Baeyens, et al.
AJOB Empirical Bioethics|October 5, 2020
Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic SequencingDanya F Vears, Pascal Borry, Julian Savulescu, et al.
Journal of Community Genetics|September 1, 2017
Readability of informed consent forms for whole-exome and whole-genome sequencingEmilia Niemiec, Danya F Vears, Pascal Borry, et al.
Familial Cancer|March 29, 2024
Clinician perspectives on policy approaches to genetic risk disclosure in familiesAmicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 28, 2022
A review of normative documents on preimplantation genetic testing: Recommendations for PGT-PMaria Siermann, Olga Tšuiko, Joris Robert Vermeesch, et al.
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