Showing results (1-10 of 206) with videos related to

Sort By:
Pageof 21
Journal of Public Health Policy|March 28, 2008
Newborn blood spot screening in four countries: stakeholder involvementBeth K Potter, Denise Avard, Brenda J Wilson
International Journal of Technology Assessment in Health Care|October 3, 2008
Guidance for considering ethical, legal, and social issues in health technology assessment: application to genetic screeningBeth K Potter, Denise Avard, Ian D Graham, et al.
Public Health Genomics|October 30, 2019
Family History Taking in Pediatric Practice: A Qualitative Interview StudyLaure Tessier, Jamie C Brehaut, Beth K Potter, et al.
Journal of Genetic Counseling|November 19, 2014
Education and parental involvement in decision-making about newborn screening: understanding goals to clarify contentBeth K Potter, Holly Etchegary, Stuart G Nicholls, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2012
Factors associated with knowledge of and satisfaction with newborn screening education: a survey of mothersMakda H Araia, Brenda J Wilson, Pranesh Chakraborty, et al.
Genome Medicine|April 4, 2009
Genomic medicine: considerations for health professionals and the publicDenise Avard, Bartha Maria Knoppers
Personalized Medicine|May 23, 2018
'Principled' personalized medicine?Bartha Maria Knoppers, Denise Avard
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|January 16, 2016
Defining the Scope of Public Engagement: Examining the "Right Not to Know" in Public Health GenomicsClarissa Allen, Karine Sénécal, Denise Avard
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|March 10, 2007
Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutationDoug Horsman, Brenda J Wilson, Denise Avard, et al.
Pageof 21