1. A survey of phenotypic features in juvenile polyposis. Issue 6 (June 1998) Authors: Desai, D C; Murday, V; Phillips, R K; Neale, K F; Milla, P; Hodgson, S V Journal: Journal of medical genetics Issue: Volume 35:Issue 6(1998) Page Start: 476 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. Biliary hypoplasia in Williams syndrome. Issue 5 (21st April 2006) Authors: O'Reilly, K; Ahmed, S F; Murday, V; McGrogan, P Journal: Archives of disease in childhood Issue: Volume 91:Issue 5(2006) Page Start: 420 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cancer and the Peutz-Jeghers syndrome. Issue 11 (November 1989) Authors: Spigelman, A D; Murday, V; Phillips, R K Journal: Gut Issue: Volume 30:Issue 11(1989) Page Start: 1588 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins. Issue 3 (23rd August 2005) Authors: Johnson, D; Morrison, N; Grant, L; Turner, T; Fantes, J; Connor, J M; Murday, V Journal: Journal of medical genetics Issue: Volume 43:Issue 3(2006) Page Start: 280 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?. Issue 6 (June 1994) Authors: Eng, C; Murday, V; Seal, S; Mohammed, S; Hodgson, S V; Chaudary, M A; Fentiman, I S; Ponder, B A; Eeles, R A Journal: Journal of medical genetics Issue: Volume 31:Issue 6(1994) Page Start: 458 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Issue 4 (31st March 2006) Authors: Hearle, N C M; Rudd, M F; Lim, W; Murday, V; Lim, A G; Phillips, R K; Lee, P W; O'Donohue, J; Morrison, P J; Norman, A; Hodgson, S V; Lucassen, A; Houlston, R S Journal: Journal of medical genetics Issue: Volume 43:Issue 4(2006) Page Start: e15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Family history of breast cancer: what do women understand and recall about their genetic risk?. Issue 9 (September 1998) Authors: Watson, M; Duvivier, V; Wade Walsh, M; Ashley, S; Davidson, J; Papaikonomou, M; Murday, V; Sacks, N; Eeles, R Journal: Journal of medical genetics Issue: Volume 35:Issue 9(1998) Page Start: 731 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic screening in patients with cardiomyopathy: experience of a new centre for the west of Scotland. (22nd September 2015) Authors: Findlay, IN; Murday, V Journal: Heart Issue: Volume 95(2009)Supplement 1 Page Start: 102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. PTEN mutations are uncommon in Proteus syndrome. Issue 7 (1st July 2001) Authors: Barker, K; Martinez, A; Wang, R; Bevan, S; Murday, V; Shipley, J; Houlston, R; Harper, J Journal: Journal of medical genetics Issue: Volume 38:Issue 7(2001) Page Start: 480 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗