1. A deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto). Issue 10 (October 1988) Authors: Cox, D W; Wills, D E; Quan, F; Ray, P N Journal: Journal of medical genetics Issue: Volume 25:Issue 10(1988) Page Start: 649 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy. Issue 6 (December 1986) Authors: Thompson, M W; Ray, P N; Belfall, B; Duff, C; Logan, C; Oss, I; Worton, R G Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Molecular deletion analysis in Duchenne muscular dystrophy. Issue 6 (December 1986) Authors: Thomas, N S; Ray, P N; Worton, R G; Harper, P S Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 509 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Monozygotic twins discordant for Aicardi syndrome. Issue 8 (August 1997) Authors: Costa, T; Greer, W; Rysiecki, G; Buncic, J R; Ray, P N Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 688 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Partial gene duplication in Duchenne and Becker muscular dystrophies. Issue 6 (June 1988) Authors: Hu, X Y; Burghes, A H; Ray, P N; Thompson, M W; Murphy, E G; Worton, R G Journal: Journal of medical genetics Issue: Volume 25:Issue 6(1988) Page Start: 369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. Issue 6 (December 1986) Authors: Kean, V M; Macleod, H L; Thompson, M W; Ray, P N; Verellen-Dumoulin, C; Worton, R G Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 491 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy. Issue 7 (July 1990) Authors: Bodrug, S E; Roberson, J R; Weiss, L; Ray, P N; Worton, R G; Van Dyke, D L Journal: Journal of medical genetics Issue: Volume 27:Issue 7(1990) Page Start: 426 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred. Issue 10 (October 1996) Authors: MacKenzie, J J; Fitzpatrick, J; Babyn, P; Ferrero, G B; Ballabio, A; Billingsley, G; Bulman, D E; Strasberg, P; Ray, P N; Costa, T Journal: Journal of medical genetics Issue: Volume 33:Issue 10(1996) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗