A New Edition of The Journal of Law, Medicine & Ethics is Available

May 19, 2014

The Journal of Law, Medicine & Ethics (Volume 42, No. 1, Spring 2014) is now available online by subscription only.

Articles include:

  • “Defining the Scope of Public Engagement: Examining the “Right Not to Know” in Public Health Genomics” by Clarissa Allen, Karine Sénécal and Denise Avard
  • “Is There a Right Time to Know? The Right Not to Know and Genetic Testing in Children” by Pascal Borry, Mahsa Shabani and Heidi Carmen Howard
  • “Autonomy, the Right Not to Know, and the Right to Know Personal Research Results: What Rights Are There, and Who Should Decide about Exceptions?” by Gert Helgesson
  • “The Right Not to Know and the Duty to Tell: The Case of Relatives” by Niklas Juth
  • “Recognizing the Right Not to Know: Conceptual, Professional, and Legal Implications” by Graeme Laurie
  • “Care Coordination and the Expansion of Nursing Scopes of Practice” by Y. Tony Yang and Mark R. Meiners

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Posted in Genetic Ethics, Journal Articles, Nursing, Public Policy

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