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. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy. Issue 6558 (22nd November 1986) Authors: Meredith, A L; Huson, S M; Lunt, P W; Sarfarazi, M; Harley, H G; Brook, J D; Shaw, D J; Harper, P S Journal: BMJ Issue: Volume 293:Issue 6558(1986) Page Start: 1353 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. Gene mapping and chromosome 19. Issue 1 (February 1986) Authors: Shaw, D J; Brook, J D; Meredith, A L; Harley, H G; Sarfarazi, M; Harper, P S Journal: Journal of medical genetics Issue: Volume 23:Issue 1(1986) Page Start: 2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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) ↗
6. 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) ↗
7. Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy. Issue 9 (September 1995) Authors: Poulton, J; Harley, H G; Dasmahapatra, J; Brown, G K; Potter, C G; Sykes, B Journal: Journal of medical genetics Issue: Volume 32:Issue 9(1995) Page Start: 732 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Issue 11 (November 1992) Authors: Myring, J; Meredith, A L; Harley, H G; Kohn, G; Norbury, G; Harper, P S; Shaw, D J Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 785 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗