1. Genetics of childhood spinal muscular atrophy. Issue 2 (June 1971) Authors: Winsor, E J; Murphy, E G; Thompson, M W; Reed, T E Journal: Journal of medical genetics Issue: Volume 8:Issue 2(1971) Page Start: 143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Incidence of salt-losing form of congenital virilizing adrenal hyperplasia. Issue 252 (April 1972) Authors: Qazi, Q H; Thompson, M W Journal: Archives of disease in childhood Issue: Volume 47:Issue 252(1972) Page Start: 302 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. 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) ↗
5. 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) ↗