Who should access germline genome sequencing? A mixed methods study of patient views

Best, Megan C., Butow, Phyllis, Jacobs, Chris, Savard, Jacqueline, Biesecker, Barbara, Ballinger, Mandy L., Bartley, Nicci, Davies, Grace, Napier, Christine E., Smit, Amelia K., Thomas, David M., Newson, Ainsley J. and And Members of the PiGeOn Project 2020, Who should access germline genome sequencing? A mixed methods study of patient views, Clinical Genetics, vol. 97, no. 2, pp. 329-337, doi: 10.1111/cge.13664.

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Title Who should access germline genome sequencing? A mixed methods study of patient views
Author(s) Best, Megan C.
Butow, Phyllis
Jacobs, Chris
Savard, JacquelineORCID iD for Savard, Jacqueline orcid.org/0000-0002-7965-6103
Biesecker, Barbara
Ballinger, Mandy L.
Bartley, Nicci
Davies, Grace
Napier, Christine E.
Smit, Amelia K.
Thomas, David M.
Newson, Ainsley J.
And Members of the PiGeOn Project
Journal name Clinical Genetics
Volume number 97
Issue number 2
Start page 329
End page 337
Total pages 9
Publisher Wiley
Place of publication London, Eng.
Publication date 2020-02
ISSN 0009-9163
1399-0004
Keyword(s) Science & Technology
Life Sciences & Biomedicine
Oncology
Genetics & Heredity
cancer
cancer risk
genome sequencing
patient views
screening
OVARIAN-CANCER
BREAST-CANCER
GENETIC TESTS
RISK
EXPERIENCES
CHALLENGES
PHYSICIANS
CLINICIAN
BENEFITS
BEHAVIOR
Members of the PiGeOn Project
Language eng
DOI 10.1111/cge.13664
Indigenous content off
Field of Research 0604 Genetics
1103 Clinical Sciences
HERDC Research category C1 Refereed article in a scholarly journal
Persistent URL http://hdl.handle.net/10536/DRO/DU:30132511

Document type: Journal Article
Collections: Faculty of Health
School of Medicine
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