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Wendy Bos

Showing results (1-10 of 5) with videos related to

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Molecular Genetics & Genomic Medicine|February 12, 2022
Informed consent practices for exome sequencing: An interview study with clinical geneticists in the NetherlandsWendy Bos, Eline M Bunnik
European Journal of Pediatrics|October 18, 2012
Ethical aspects of clinical research with minorsWendy Bos, Krista Tromp, Dick Tibboel, et al.
Bioethics|October 21, 2015
Morally Relevant Similarities and Differences Between Children and Dementia Patients as Research Subjects: Representation in Legal Documents and Ethical GuidelinesKarin Jongsma, Wendy Bos, Suzanne van de Vathorst
Journal of Medical Ethics|December 10, 2016
To stop or not to stop: dissent and undue burden as reasons to stop participation in paediatric researchWendy Bos, Anna Westra, Inez de Beaufort, et al.
Pediatrics|November 11, 2015
Risks in a Trial of an Innovative Treatment of Duchenne Muscular DystrophyWendy Bos, Anna E Westra, Wim Pinxten, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Molecular Genetics & Genomic Medicine|February 12, 2022
Informed consent practices for exome sequencing: An interview study with clinical geneticists in the NetherlandsWendy Bos, Eline M Bunnik
European Journal of Pediatrics|October 18, 2012
Ethical aspects of clinical research with minorsWendy Bos, Krista Tromp, Dick Tibboel, et al.
Bioethics|October 21, 2015
Morally Relevant Similarities and Differences Between Children and Dementia Patients as Research Subjects: Representation in Legal Documents and Ethical GuidelinesKarin Jongsma, Wendy Bos, Suzanne van de Vathorst
Journal of Medical Ethics|December 10, 2016
To stop or not to stop: dissent and undue burden as reasons to stop participation in paediatric researchWendy Bos, Anna Westra, Inez de Beaufort, et al.
Pediatrics|November 11, 2015
Risks in a Trial of an Innovative Treatment of Duchenne Muscular DystrophyWendy Bos, Anna E Westra, Wim Pinxten, et al.
Pageof 1