1. 21-hydroxylase deficiency families with HLA identical affected and unaffected sibs. Issue 1 (January 1989) Authors: Sinnott, P J; Dyer, P A; Price, D A; Harris, R; Strachan, T Journal: Journal of medical genetics Issue: Volume 26:Issue 1(1989) Page Start: 10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 5 Quality Improvement Project (QIP): A Teamwork Approach to Optimise Fluid Intake in Older Inpatients #ButFirstADrink. (16th March 2021) Authors: Vourliotis, N; Grimshaw, K; Harris, R Journal: Age and ageing Issue: Volume 50(2021)Supplement 1 Page Start: i1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 74PCommon and rare DPYD variants are predictive for 5FU/capecitabine (5FU) toxicity: The MRC COIN and COIN-B trials. (23rd October 2018) Authors: Madi, A; Fisher, D; Maughan, T S; Colley, J P; Meade, A M; Maynard, J; Humphreys, V; Wasan, H; Adams, R A; Idziaszczyk, S; Harris, R; Kaplan, R S; Cheadle, J P Journal: Annals of oncology Issue: Volume 29(2018)Supplement 8 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A clinical study of type 1 neurofibromatosis in north west England. Issue 3 (1st March 1999) Authors: McGaughran, J M; Harris, D I; Donnai, D; Teare, D; MacLeod, R; Westerbeek, R; Kingston, H; Super, M; Harris, R; Evans, D G R Journal: Journal of medical genetics Issue: Volume 36:Issue 3(1999) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A comparison of methohexitone and thiopentone in electrocorticography. Issue 1 (February 1970) Authors: Paul, R; Harris, R Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 33:Issue 1(1970) Page Start: 100 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies. Issue 6 (December 1979) Authors: Donnai, D; Harris, R Journal: Journal of medical genetics Issue: Volume 16:Issue 6(1979) Page Start: 483 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Teare, D; Newton, V; Strachan, T; Ramsden, R; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 841 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Newton, V; Strachan, T; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 847 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A register based system for gene tracking in Duchenne muscular dystrophy. Issue 6 (December 1986) Authors: Read, A P; Kerzin-Storrar, L; Mountford, R C; Elles, R G; Harris, R Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 581 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party. Issue 6 (December 1978) Authors: Emery, A E; Brough, C; Crawfurd, M; Harper, P; Harris, R; Oakshott, G Journal: Journal of medical genetics Issue: Volume 15:Issue 6(1978) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗