1. Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes. Issue 5 (May 1990) Authors: Cooke, A; Lanyon, W G; Wilcox, D E; Dornan, E S; Kataki, A; Gillard, E F; McWhinnie, A J; Morris, A; Ferguson-Smith, M A; Connor, J M Journal: Journal of medical genetics Issue: Volume 27:Issue 5(1990) Page Start: 292 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis. Issue 2 (February 1987) Authors: Cooke, A; Tolmie, J; Darlington, W; Boyd, E; Thomson, R; Ferguson-Smith, M A Journal: Journal of medical genetics Issue: Volume 24:Issue 2(1987) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Connective tissue abnormalities in MRL/1 mice. Issue 6 (June 1986) Authors: Edwards, J C; Cooke, A; Moore, A R; Collins, C; Hay, F; Willoughby, D A Journal: Annals of the rheumatic diseases Issue: Volume 45:Issue 6(1986) Page Start: 512 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Diagnosis in Prader-Willi syndrome. Issue 5 (November 1994) Authors: Chu, C E; Cooke, A; Stephenson, J B; Tolmie, J L; Clarke, B; Parry-Jones, W L; Connor, J M; Donaldson, M D Journal: Archives of disease in childhood Issue: Volume 71:Issue 5(1994) Page Start: 441 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families. Issue 6 (December 1996) Authors: Ahmed, M A; Reid, E; Cooke, A; Arngrímsson, R; Tolmie, J L; Stephenson, J B Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 61:Issue 6(1996) Page Start: 616 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study. Issue 3 (March 1996) Authors: Reid, E; Morrison, N; Barron, L; Boyd, E; Cooke, A; Fielding, D; Tolmie, J L Journal: Journal of medical genetics Issue: Volume 33:Issue 3(1996) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. G359(P) Characterising the disease presentations of lch over 10 yr at a uk ptc. (12th March 2018) Authors: Mitchell, AFM; Ramanujachar, R; Gray, J; Nicolin, G; Uparkhar, U; Vadgama, B; Cooke, A Journal: Archives of disease in childhood Issue: Volume 103:Supplement 1(2018) Page Start: A146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Growth of the uterus. Issue 4 (October 1996) Authors: Bridges, N A; Cooke, A; Healy, M J; Hindmarsh, P C; Brook, C G Journal: Archives of disease in childhood Issue: Volume 75:Issue 4(1996) Page Start: 330 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Lateral deviation of toes requires lateral thinking. Issue 1 (22nd December 2008) Authors: Mangalore Devdas, J; Campbell-Hewson, Q; Friswell, M; Gupta, A; Featherstone, T; Cooke, A; DeKiewiet, G; Hopper, N W Journal: Archives of disease in childhood Issue: Volume 94:Issue 1(2009) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Parents' experiences and expectations of care in pregnancy after stillbirth or neonatal death: a metasynthesis. (4th March 2014) Authors: Mills, TA; Ricklesford, C; Cooke, A; Heazell, AEP; Whitworth, M; Lavender, T Journal: BJOG Issue: Volume 121:Number 8(2014:Aug.) Page Start: 943 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗