1. OPUS at UTS

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Issue DateTitleAuthor(s)
2021-09Beyond platitudes: a qualitative study of Australian Aboriginal people's perspectives on biobanking.Hermes, A; Wiersma, M; Kerridge, I; Easteal, S; Light, E; Dive, L; Lipworth, W
2019-10Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy.Sexton, A; Gargan, B; Taylor, J; Bogwitz, M; Winship, I
2022-11-17Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia.Monohan, K; Purvis, R; Sexton, A; Kentwell, M; Thet, M; Stafford, L; Forrest, L
2020-08"It wasn't just for me": Motivations and implications of genetic testing for women at a low risk of hereditary breast and ovarian cancer syndrome.Gill, G; Beard, C; Storey, K; Taylor, S; Sexton, A
2020-08Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot study.Pieper, E; Sexton, A; Ryan, MM; Forbes, R
2022-01-01Ethical considerations in gene selection for reproductive carrier screening.Dive, L; Archibald, AD; Newson, AJ
2022-03Ethical aspects of the changing landscape for spinal muscular atrophy management in Australia.Newson, AJ; Dive, L; Cini, J; Hurley, E; Farrar, MA
2022-01-01My Research Results: a program to facilitate return of clinically actionable genomic research findings.Willis, AM; Terrill, B; Pearce, A; McEwen, A; Ballinger, ML; Young, M-A
2021-10Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review.Crook, A; Jacobs, C; Newton-John, T; Richardson, E; McEwen, A
2022-04Genetic counselling and testing for neurodegenerative disorders using a proposed standard of practice for ALS/MND: diagnostic testing comes first.Crook, A; McEwen, A
Results 31-40 of 67 (Search time: 0.011 seconds).

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