Australians’ views and experience of personal genomic testing: survey findings from the Genioz study
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1476-5438
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Australians’ views and experience of personal genomic testing: survey findings from the Genioz study ; day:21 ; month:1 ; year:2019 ; pages:1-10
European journal of human genetics ; (21.1.2019), 1-10
- Creator
-
Savard, Jacqueline
Hickerton, Chriselle
Tytherleigh, Rigan
Terrill, Bronwyn
Turbitt, Erin
Newson, Ainsley J.
Wilson, Brenda
Gray, Kathleen
Gaff, Clara
Middleton, Anna
Stackpoole, Elaine
Metcalfe, Sylvia A.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41431-018-0325-x
- URN
-
urn:nbn:de:101:1-2019022400162994121913
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:49 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Savard, Jacqueline
- Hickerton, Chriselle
- Tytherleigh, Rigan
- Terrill, Bronwyn
- Turbitt, Erin
- Newson, Ainsley J.
- Wilson, Brenda
- Gray, Kathleen
- Gaff, Clara
- Middleton, Anna
- Stackpoole, Elaine
- Metcalfe, Sylvia A.
- SpringerLink (Online service)
Other Objects (12)
Australians’ views on personal genomic testing: focus group findings from the Genioz study
The landscape of genomic structural variation in Indigenous Australians
Seven little Australians
Financial Stress and Indigenous Australians
Financial stress and Indigenous Australians
Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK
Genomic findings in schizophrenia and their implications
Understanding Indigenous Australians’ experiences of cancer care: stakeholders’ views on what to measure and how to measure it
Ethical considerations in prenatal genomic testing
Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study
In search of an identity : essays and ideas on Anglo-Australians, German-Australians and others
Australians’ views on personal genomic testing: focus group findings from the Genioz study
The landscape of genomic structural variation in Indigenous Australians
Seven little Australians
Financial Stress and Indigenous Australians
Financial stress and Indigenous Australians
Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK
Genomic findings in schizophrenia and their implications
Understanding Indigenous Australians’ experiences of cancer care: stakeholders’ views on what to measure and how to measure it
Ethical considerations in prenatal genomic testing
Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study
In search of an identity : essays and ideas on Anglo-Australians, German-Australians and others
Australians’ views on personal genomic testing: focus group findings from the Genioz study
The landscape of genomic structural variation in Indigenous Australians
Seven little Australians
Financial Stress and Indigenous Australians
Financial stress and Indigenous Australians
Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK
Genomic findings in schizophrenia and their implications
Understanding Indigenous Australians’ experiences of cancer care: stakeholders’ views on what to measure and how to measure it
Ethical considerations in prenatal genomic testing
Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study