1. An interstitial deletion of chromosome 7(q35). Issue 9 (September 1994) Authors: Fagan, K; Kennedy, C; Roddick, L; Colley, A Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 738 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?. Issue 1 (January 1997) Authors: Worthington, S; Colley, A; Fagan, K; Dai, K; Lipson, A H Journal: Journal of medical genetics Issue: Volume 34:Issue 1(1997) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion. Issue 2 (February 1996) Authors: Smith, A; Wiles, C; Haan, E; McGill, J; Wallace, G; Dixon, J; Selby, R; Colley, A; Marks, R; Trent, R J Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 107 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. De novo ring chromosome 3: a new case with a mild phenotype. Issue 8 (August 1991) Authors: McKinley, M; Colley, A; Sinclair, P; Donnai, D; Andrews, T Journal: Journal of medical genetics Issue: Volume 28:Issue 8(1991) Page Start: 536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Dominantly inherited unilateral retinal dysplasia. Issue 6 (June 1993) Authors: Lloyd, I C; Colley, A; Tullo, A B; Bonshek, R Journal: British journal of ophthalmology Issue: Volume 77:Issue 6(1993) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Ectopia lentis et pupillae: the genetic aspects and differential diagnosis. Issue 11 (November 1991) Authors: Colley, A; Lloyd, I C; Ridgway, A; Donnai, D Journal: Journal of medical genetics Issue: Volume 28:Issue 11(1991) Page Start: 791 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis. Issue 6 (19th February 2008) Authors: Hadfield, K D; Newman, W G; Bowers, N L; Wallace, A; Bolger, C; Colley, A; McCann, E; Trump, D; Prescott, T; Evans, D G R Journal: Journal of medical genetics Issue: Volume 45:Issue 6(2008) Page Start: 332 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families. Issue 7 (July 1993) Authors: Benjamin, C M; Colley, A; Donnai, D; Kingston, H; Harris, R; Kerzin-Storrar, L Journal: Journal of medical genetics Issue: Volume 30:Issue 7(1993) Page Start: 567 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel mutations of the PRKAR1A gene in patients with acrodysostosis. (21st February 2013) Authors: Muhn, F; Klopocki, E; Graul‐Neumann, L; Uhrig, S; Colley, A; Castori, M; Lankes, E; Henn, W; Gruber‐Sedlmayr, U; Seifert, W; Horn, D Journal: Clinical genetics Issue: Volume 84:Number 6(2013:Dec.) Page Start: 531 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Unbalanced 13;18 translocation and Williams syndrome. Issue 1 (January 1992) Authors: Colley, A; Thakker, Y; Ward, H; Donnai, D Journal: Journal of medical genetics Issue: Volume 29:Issue 1(1992) Page Start: 63 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗