1. An investigation of patients' motivations for their participation in genetics-related research. Issue 1 (21st December 2009) Authors: Hallowell, N; Cooke, S; Crawford, G; Lucassen, A; Parker, M; Snowdon, C Journal: Journal of medical ethics Issue: Volume 36:Issue 1(2010) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information. Issue 2 (1st April 2003) Authors: Hallowell, N; Foster, C; Eeles, R; Ardern-Jones, A; Murday, V; Watson, M Journal: Journal of medical ethics Issue: Volume 29:Issue 2(2003) Page Start: 74 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research. Issue 9 (29th August 2008) Authors: Ponder, M; Statham, H; Hallowell, N; Moon, J A; Richards, M; Raymond, F L Journal: Journal of medical ethics Issue: Volume 34:Issue 9(2008) Page Start: 690 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Healthcare professionals' and researchers' understanding of cancer genetics activities: a qualitative interview study. Issue 2 (30th January 2009) Authors: Hallowell, N; Cooke, S; Crawford, G; Parker, M; Lucassen, A Journal: Journal of medical ethics Issue: Volume 35:Issue 2(2009) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗