1. A boy with developmental delay and a maternally inherited deletion in 15q11q13. Issue 5 (May 1996) Authors: King, M; Hardy, C; Asenbauer, B; Kilpatrick, M; Webb, T Journal: Journal of medical genetics Issue: Volume 33:Issue 5(1996) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome. Issue 3 (March 1995) Authors: Webb, T; Clarke, D; Hardy, C A; Kilpatrick, M W; Corbett, J; Dahlitz, M Journal: Journal of medical genetics Issue: Volume 32:Issue 3(1995) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome. Issue 6 (June 1994) Authors: Vickers, S; Dahlitz, M; Hardy, C; Kilpatrick, M; Webb, T Journal: Journal of medical genetics Issue: Volume 31:Issue 6(1994) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Advertising alcohol: does the Advertising Standards Authority exercise any control?. Issue 6452 (27th October 1984) Authors: Webb, T Journal: BMJ Issue: Volume 289:Issue 6452(1984) Page Start: 1145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Alcoholism: time for action. Issue 6280 (13th June 1981) Authors: Webb, T Journal: BMJ Issue: Volume 282:Issue 6280(1981) Page Start: 1969 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13. Issue 12 (December 1992) Authors: Webb, T; Clayton-Smith, J; Cheng, X J; Knoll, J H; Lalande, M; Pembrey, M E; Malcolm, S Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 921 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Developmental delay and the methyl binding genes. Issue 2 (1st February 2003) Authors: Turner, H; MacDonald, F; Warburton, S; Latif, F; Webb, T Journal: Journal of medical genetics Issue: Volume 40:Issue 2(2003) Page Start: e13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. Issue 1 (17th August 2011) Authors: Alner, K; Hyare, H; Mead, S; Rudge, P; Wroe, S; Rohrer, J D; Ridgway, G R; Ourselin, S; Clarkson, M; Hunt, H; Fox, N C; Webb, T; Collinge, J; Cipolotti, L Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 1(2012) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Do drug dependence clinics work?. Issue 6300 (31st October 1981) Authors: Webb, T Journal: BMJ Issue: Volume 283:Issue 6300(1981) Page Start: 1185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Do drug dependence clinics work?. Issue 6305 (5th December 1981) Authors: Webb, T Journal: BMJ Issue: Volume 283:Issue 6305(1981) Page Start: 1548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗