1. Age at onset in Huntington's disease and methylation at D4S95. Issue 3 (March 1993) Authors: Reik, W; Maher, E R; Morrison, P J; Harding, A E; Simpson, S A Journal: Journal of medical genetics Issue: Volume 30:Issue 3(1993) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART). Issue 1 (1st January 2003) Authors: Maher, E R; Brueton, L A; Bowdin, S C; Luharia, A; Cooper, W; Cole, T R; Macdonald, F; Sampson, J R; Barratt, C L; Reik, W; Hawkins, M M Journal: Journal of medical genetics Issue: Volume 40:Issue 1(2003) Page Start: 62 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome. Issue 5 (May 1997) Authors: Catchpoole, D; Lam, W W; Valler, D; Temple, I K; Joyce, J A; Reik, W; Schofield, P N; Maher, E R Journal: Journal of medical genetics Issue: Volume 34:Issue 5(1997) Page Start: 353 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea. Issue 12 (December 1988) Authors: Reik, W Journal: Journal of medical genetics Issue: Volume 25:Issue 12(1988) Page Start: 805 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome. Issue 11 (19th November 2003) Authors: Diaz-Meyer, N; Day, C D; Khatod, K; Maher, E R; Cooper, W; Reik, W; Junien, C; Graham, G; Algar, E; Der Kaloustian, V M; Higgins, M J Journal: Journal of medical genetics Issue: Volume 40:Issue 11(2003) Page Start: 797 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗