1. Clinical features of pulmonary arterial hypertension in young people with an ALK1 mutation and hereditary haemorrhagic telangiectasia. Issue 7 (8th April 2009) Authors: Smoot, L B; Obler, D; McElhinney, D B; Boardman, K; Wu, B-L; Lip, V; Mullen, M P Journal: Archives of disease in childhood Issue: Volume 94:Issue 7(2009) Page Start: 506 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. Issue 4 (19th September 2008) Authors: Miller, D T; Shen, Y; Weiss, L A; Korn, J; Anselm, I; Bridgemohan, C; Cox, G F; Dickinson, H; Gentile, J; Harris, D J; Hegde, V; Hundley, R; Khwaja, O; Kothare, S; Luedke, C; Nasir, R; Poduri, A; Prasad, K; Raffalli, P; Reinhard, A Journal: Journal of medical genetics Issue: Volume 46:Issue 4(2009) Page Start: 242 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗