1. A study of DNA methylation in myotonic dystrophy. Issue 3 (March 1993) Authors: Shaw, D J; Chaudhary, S; Rundle, S A; Crow, S; Brook, J D; Harper, P S; Harley, H G Journal: Journal of medical genetics Issue: Volume 30:Issue 3(1993) Page Start: 189 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cataract and myotonic dystrophy: the role of molecular diagnosis. Issue 9 (September 1993) Authors: Reardon, W; MacMillan, J C; Myring, J; Harley, H G; Rundle, S A; Beck, L; Harper, P S; Shaw, D J Journal: British journal of ophthalmology Issue: Volume 77:Issue 9(1993) Page Start: 579 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of new DNA markers close to the myotonic dystrophy locus. Issue 2 (February 1991) Authors: Brook, J D; Harley, H G; Walsh, K V; Rundle, S A; Siciliano, M J; Harper, P S; Shaw, D J Journal: Journal of medical genetics Issue: Volume 28:Issue 2(1991) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Minimal expression of myotonic dystrophy: a clinical and molecular analysis. Issue 11 (November 1992) Authors: Reardon, W; Harley, H G; Brook, J D; Rundle, S A; Crow, S; Harper, P S; Shaw, D J Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 770 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗