1. Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences. Issue 4 (August 1983) Authors: O'Brien, T; Harper, P S; Davies, K E; Murray, J M; Sarfarazi, M; Williamson, R Journal: Journal of medical genetics Issue: Volume 20:Issue 4(1983) Page Start: 249 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy. Issue 12 (December 1991) Authors: Love, D R; Flint, T J; Genet, S A; Middleton-Price, H R; Davies, K E Journal: Journal of medical genetics Issue: Volume 28:Issue 12(1991) Page Start: 860 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Bridging markers defining the map position of X linked hypophosphataemic rickets. Issue 12 (December 1987) Authors: Thakker, R V; Read, A P; Davies, K E; Whyte, M P; Weksberg, R; Glorieux, F; Davies, M; Mountford, R C; Harris, R; King, A Journal: Journal of medical genetics Issue: Volume 24:Issue 12(1987) Page Start: 756 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms. Issue 6 (December 1986) Authors: Lindlöf, M; Kääriäinen, H; Davies, K E; de la Chapelle, A Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 560 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy. Issue 3 (March 1984) Authors: Pembrey, M E; Davies, K E; Winter, R M; Elles, R G; Williamson, R; Fazzone, T A; Walker, C Journal: Archives of disease in childhood Issue: Volume 59:Issue 3(1984) Page Start: 208 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. DNA testing for fragile X syndrome in schools for learning difficulties. Issue 1 (January 1995) Authors: Slaney, S F; Wilkie, A O; Hirst, M C; Charlton, R; McKinley, M; Pointon, J; Christodoulou, Z; Huson, S M; Davies, K E Journal: Archives of disease in childhood Issue: Volume 72:Issue 1(1995) Page Start: 33 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Gene deletions in spinal muscular atrophy. Issue 2 (February 1996) Authors: Rodrigues, N R; Owen, N; Talbot, K; Patel, S; Muntoni, F; Ignatius, J; Dubowitz, V; Davies, K E Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗
9. Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. Issue 2 (February 1995) Authors: Daniels, R J; Campbell, L; Rodrigues, N R; Francis, M J; Morrison, K E; McLean, M; MacKenzie, A; Ignatius, J; Dubowitz, V; Davies, K E Journal: Journal of medical genetics Issue: Volume 32:Issue 2(1995) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genotype prediction in the fragile X syndrome. Issue 12 (December 1991) Authors: Hirst, M C; Nakahori, Y; Knight, S J; Schwartz, C; Thibodeau, S N; Roche, A; Flint, T J; Connor, J M; Fryns, J P; Davies, K E Journal: Journal of medical genetics Issue: Volume 28:Issue 12(1991) Page Start: 824 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗