Old Challenges or New Issues? Genetic Health Professionals’ Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing

Danya F. Vearsa Melbourne Law School, University of Melbourne, Parkville, Australia;b Biomedical Ethics Research Group, Murdoch Children’s Research Institute, Parkville, Australia;c Department of Public Health and Primary Care, Center for Biomedical Ethics and Law, Leuven, Belgium;d Leuven Institute for Human Genetics and Society, Leuven, BelgiumCorrespondence[email protected]
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Pascal Borryc Department of Public Health and Primary Care, Center for Biomedical Ethics and Law, Leuven, Belgium;d Leuven Institute for Human Genetics and Society, Leuven, Belgium

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Julian Savulescua Melbourne Law School, University of Melbourne, Parkville, Australia;b Biomedical Ethics Research Group, Murdoch Children’s Research Institute, Parkville, Australia;e Oxford Uehiro Centre for Practical Ethics, University of Oxford, Oxford, UK;f Wellcome Centre for Ethics and Humanities, University of Oxford, Oxford, UKView further author information

Julian J. Koplina Melbourne Law School, University of Melbourne, Parkville, Australia;b Biomedical Ethics Research Group, Murdoch Children’s Research Institute, Parkville, AustraliaView further author information

Old Challenges or New Issues? Genetic Health Professionals’ Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing

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Old Challenges or New Issues? Genetic Health Professionals’ Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing

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