1. A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II. Issue 10 (October 1998) Authors: Richards, A J; Martin, S; Nicholls, A C; Harrison, J B; Pope, F M; Burrows, N P Journal: Journal of medical genetics Issue: Volume 35:Issue 10(1998) Page Start: 846 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A T+6 to C+6 mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV. Issue 5 (May 1993) Authors: Lloyd, J; Narcisi, P; Richards, A; Pope, F M Journal: Journal of medical genetics Issue: Volume 30:Issue 5(1993) Page Start: 376 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndrome. Issue 4 (April 1985) Authors: Ayres, J G; Pope, F M; Reidy, J F; Clark, T J Journal: Thorax Issue: Volume 40:Issue 4(1985) Page Start: 300 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. AIDS: Modern Concepts and Therapeutic challenges. Issue 4 (April 1987) Authors: Pope, F M Journal: Archives of disease in childhood Issue: Volume 62:Issue 4(1987) Page Start: 434 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An abnormal collagen alpha chain containing cysteine in autosomal dominant osteogenesis imperfecta. Issue 6411 (14th January 1984) Authors: Nicholls, A C; Pope, F M; Craig, D Journal: BMJ Issue: Volume 288:Issue 6411(1984) Page Start: 112 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. An exclusion map of Marfan syndrome. Issue 2 (February 1990) Authors: Blanton, S H; Sarfarazi, M; Eiberg, H; de Groote, J; Farndon, P A; Kilpatrick, M W; Child, A H; Pope, F M; Peltonen, L; Francomano, C A Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome. Issue 11 (November 1996) Authors: Nicholls, A C; Oliver, J E; McCarron, S; Harrison, J B; Greenspan, D S; Pope, F M Journal: Journal of medical genetics Issue: Volume 33:Issue 11(1996) Page Start: 940 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Angioid streaks in Jamaican patients with homozygous sickle cell disease. Issue 5 (May 1981) Authors: Hamilton, A M; Pope, F M; Condon, P I; Slavin, G; Sowter, C; Ford, S; Hayes, R J; Serjeant, G R Journal: British journal of ophthalmology Issue: Volume 65:Issue 5(1981) Page Start: 341 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV. Issue 7 (July 1991) Authors: Richards, A J; Lloyd, J C; Ward, P N; De Paepe, A; Narcisi, P; Pope, F M Journal: Journal of medical genetics Issue: Volume 28:Issue 7(1991) Page Start: 458 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. Issue 4 (August 1986) Authors: Pope, F M; Nicolls, A C; Osse, G; Lee, K W Journal: Journal of medical genetics Issue: Volume 23:Issue 4(1986) Page Start: 377 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗