1. A locus for primary ciliary dyskinesia maps to chromosome 19q. Issue 4 (1st April 2000) Authors: Meeks, M; Walne, A; Spiden, S; Simpson, H; Mussaffi-Georgy, H; Hamam, H D; Fehaid, E L; Cheehab, M; Al-Dabbagh, M; Polak-Charcon, S; Blau, H; O'Rawe, A; Mitchison, H M; Gardiner, R M; Chung, E Journal: Journal of medical genetics Issue: Volume 37:Issue 4(2000) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. Issue 5 (May 1996) Authors: Elmslie, F V; Hutchings, S M; Spencer, V; Curtis, A; Covanis, T; Gardiner, R M; Rees, M Journal: Journal of medical genetics Issue: Volume 33:Issue 5(1996) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy. Issue 11 (November 1991) Authors: Poulton, J; Deadman, M E; Bronte-Stewart, J; Foulds, W S; Gardiner, R M Journal: Journal of medical genetics Issue: Volume 28:Issue 11(1991) Page Start: 765 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cerebral blood flow in diabetes mellitus. Issue 6136 (19th August 1978) Authors: Gardiner, R M Journal: BMJ Issue: Volume 2:Issue 6136(1978) Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Ceroid-Lipofuscinoses. Batten Disease and Allied Disorders. Issue 8 (August 1989) Authors: Gardiner, R M Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Congenital haemolytic anaemia associated with abnormal inducible red cell cation permeability. Issue 7 (July 1983) Authors: Gardiner, R M; Barnes, N D; Ellory, J C Journal: Archives of disease in childhood Issue: Volume 58:Issue 7(1983) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genes and epilepsy. Issue 9 (September 1990) Authors: Gardiner, R M Journal: Journal of medical genetics Issue: Volume 27:Issue 9(1990) Page Start: 537 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Late Onset Neurometabolic Genetic Disorders. Issue 2 (February 1993) Authors: Gardiner, R M Journal: Journal of medical genetics Issue: Volume 30:Issue 2(1993) Page Start: 176 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region. Issue 5 (May 1993) Authors: Chung, E; Coffey, R; Parker, K; Tam, P; Pembrey, M E; Gardiner, R M Journal: Journal of medical genetics Issue: Volume 30:Issue 5(1993) Page Start: 393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Locus heterogeneity in progressive familial intrahepatic cholestasis. Issue 10 (October 1996) Authors: Strautnieks, S S; Kagalwalla, A F; Tanner, M S; Gardiner, R M; Thompson, R J Journal: Journal of medical genetics Issue: Volume 33:Issue 10(1996) Page Start: 833 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗