1. Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome. Issue 12 (December 1993) Authors: Glass, I A; Good, P; Coleman, M P; Fullwood, P; Giles, M G; Lindsay, S; Nemeth, A H; Davies, K E; Willshaw, H A; Fielder, A Journal: Journal of medical genetics Issue: Volume 30:Issue 12(1993) Page Start: 1044 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. No evidence for uniparental disomy as a common cause of Sotos syndrome. Issue 1 (January 1997) Authors: Smith, M; Fullwood, P; Qi, Y; Palmer, S; Upadhyaya, M; Cole, T Journal: Journal of medical genetics Issue: Volume 34:Issue 1(1997) Page Start: 10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Role of chromosome 3p12–p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis. Issue 3 (1st June 2000) Authors: Martinez, A; Fullwood, P; Kondo, K; Kishida, T; Yao, M; Maher, E R; Latif, F Journal: Journal of clinical pathology Issue: Volume 53:Issue 3(2000) Page Start: 137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis. Issue 3 (March 1993) Authors: Fullwood, P; Jones, J; Bundey, S; Dudgeon, J; Fielder, A R; Kilpatrick, M W Journal: British journal of ophthalmology Issue: Volume 77:Issue 3(1993) Page Start: 168 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗