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Journal of Bioethical Inquiry
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November 22, 2017
Reflecting Before Testing : Comment on "Personal Genomic Testing, Genetic Inheritance, and Uncertainty"
Jacqueline Savard
Narrative Inquiry in Bioethics
|
January 12, 2016
A Test Unlike Any Other
Jacqueline Savard
Journal of Law and Medicine
|
April 23, 2013
Epidemiology, quality control and consumer access in the medical marketplace: the changing landscape of human genetic technology regulation in Australia
Jacqueline Savard
Journal of Bioethical Inquiry
|
March 22, 2013
Personalised medicine: a critique on the future of health care
Jacqueline Savard
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
August 26, 2020
Human Genetics Society of Australasia Position Statement: Online DNA Testing
Jacqueline Savard, Bronwyn Terrill, Kate Dunlop, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
January 25, 2022
Human Genetics Society of Australasia Position Statement: Use of Human Genetic and Genomic Information in Healthcare Settings
Samantha Ayres, Jackie Boyle, Ainsley J Newson, et al.
AJOB Empirical Bioethics
|
December 31, 2019
From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
Jacqueline Savard, Chriselle Hickerton, Sylvia A Metcalfe, et al.
European Journal of Human Genetics : EJHG
|
May 1, 2018
Australians' views on personal genomic testing: focus group findings from the Genioz study
Sylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
Studies in Health Technology and Informatics
|
January 4, 2018
Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing
Kathleen Gray, Remya Stephen, Bronwyn Terrill, et al.
Narrative Inquiry in Bioethics
|
August 14, 2018
Narrative Symposium: Patient and Research Participant experiences with Genetic Testing
Dena Davis, Sarah Foye, Sarah M Hartz, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Journal of Bioethical Inquiry
|
November 22, 2017
Reflecting Before Testing : Comment on "Personal Genomic Testing, Genetic Inheritance, and Uncertainty"
Jacqueline Savard
Narrative Inquiry in Bioethics
|
January 12, 2016
A Test Unlike Any Other
Jacqueline Savard
Journal of Law and Medicine
|
April 23, 2013
Epidemiology, quality control and consumer access in the medical marketplace: the changing landscape of human genetic technology regulation in Australia
Jacqueline Savard
Journal of Bioethical Inquiry
|
March 22, 2013
Personalised medicine: a critique on the future of health care
Jacqueline Savard
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
August 26, 2020
Human Genetics Society of Australasia Position Statement: Online DNA Testing
Jacqueline Savard, Bronwyn Terrill, Kate Dunlop, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
January 25, 2022
Human Genetics Society of Australasia Position Statement: Use of Human Genetic and Genomic Information in Healthcare Settings
Samantha Ayres, Jackie Boyle, Ainsley J Newson, et al.
AJOB Empirical Bioethics
|
December 31, 2019
From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
Jacqueline Savard, Chriselle Hickerton, Sylvia A Metcalfe, et al.
European Journal of Human Genetics : EJHG
|
May 1, 2018
Australians' views on personal genomic testing: focus group findings from the Genioz study
Sylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
Studies in Health Technology and Informatics
|
January 4, 2018
Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing
Kathleen Gray, Remya Stephen, Bronwyn Terrill, et al.
Narrative Inquiry in Bioethics
|
August 14, 2018
Narrative Symposium: Patient and Research Participant experiences with Genetic Testing
Dena Davis, Sarah Foye, Sarah M Hartz, et al.
Page
of 3