1. 106 Evaluation of participant feedback from a group based pain education sessions for young people aged between 9–18 years old and their parents. (4th October 2017) Authors: Lilley, S; Peters, J; Grey, S; Samuel, M; Sapochnik, M; McCarthy, K; Keen, K; Jay, M; Howard, R Journal: Archives of disease in childhood Issue: Volume 102(2017)Supplement 3 Page Start: A30 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom. Issue 7 (July 1990) Authors: Onadim, Z O; Mitchell, C D; Rutland, P C; Buckle, B G; Jay, M; Hungerford, J L; Harper, K; Cowell, J K Journal: Archives of disease in childhood Issue: Volume 65:Issue 7(1990)Spec No Page Start: 651 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression. Issue 1 (January 1995) Authors: Kim, R Y; Fitzke, F W; Moore, A T; Jay, M; Inglehearn, C; Arden, G B; Bhattacharya, S S; Bird, A C Journal: British journal of ophthalmology Issue: Volume 79:Issue 1(1995) Page Start: 23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study. Issue 8 (August 1993) Authors: Moore, A T; Fitzke, F; Jay, M; Arden, G B; Inglehearn, C F; Keen, T J; Bhattacharya, S S; Bird, A C Journal: British journal of ophthalmology Issue: Volume 77:Issue 8(1993) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q. Issue 9 (September 1995) Authors: Evans, K; al-Maghtheh, M; Fitzke, F W; Moore, A T; Jay, M; Inglehearn, C F; Arden, G B; Bird, A C Journal: British journal of ophthalmology Issue: Volume 79:Issue 9(1995) Page Start: 841 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred. Issue 7 (July 1991) Authors: Wright, A F; Bhattacharya, S S; Aldred, M A; Jay, M; Carothers, A D; Thomas, N S; Bird, A C; Jay, B; Evans, H J Journal: Journal of medical genetics Issue: Volume 28:Issue 7(1991) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Health and climate change. (15th September 2009) Authors: Jay, M; Marmot, M G Journal: BMJ Issue: Volume 339(2009) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Linkage refinement localises Sorsby fundus dystrophy between markers D22S275 and D22S278. Issue 3 (March 1995) Authors: Gregory, C Y; Wijesuriya, S; Evans, K; Jay, M; Bird, A C; Bhattacharya, S S Journal: Journal of medical genetics Issue: Volume 32:Issue 3(1995) Page Start: 240 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Linkage studies and deletion screening in choroideremia. Issue 8 (August 1990) Authors: Wright, A F; Nussbaum, R L; Bhattacharya, S S; Jay, M; Lesko, J G; Evans, H J; Jay, B Journal: Journal of medical genetics Issue: Volume 27:Issue 8(1990) Page Start: 496 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records. Issue 12 (December 1992) Authors: Jay, M; Bird, A C; Moore, A N; Jay, B Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 906 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗