1. Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis. Issue 11 (November 1989) Authors: al-Gazali, L I; Arthur, R J; Lamb, J T; Hammer, H M; Coker, T P; Hirschmann, P N; Gibbs, J; Mueller, R F Journal: Journal of medical genetics Issue: Volume 26:Issue 11(1989) Page Start: 694 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Linkage of a medium sized Scottish autosomal dominant retinitis pigmentosa family to chromosome 7q. Issue 8 (August 1996) Authors: Mohamed, Z; Bell, C; Hammer, H M; Converse, C A; Esakowitz, L; Haites, N E Journal: Journal of medical genetics Issue: Volume 33:Issue 8(1996) Page Start: 714 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Misleading aspiration biopsy in combined intraocular pathology. Issue 5 (May 1995) Authors: Sekundo, W; Lee, W R; Hammer, H M Journal: British journal of ophthalmology Issue: Volume 79:Issue 5(1995) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Rhodopsin mutations in a Scottish retinitis pigmentosa population, including a novel splice site mutation in intron four. Issue 12 (December 1994) Authors: Bell, C; Converse, C A; Hammer, H M; Osborne, A; Haites, N E Journal: British journal of ophthalmology Issue: Volume 78:Issue 12(1994) Page Start: 933 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗