1. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. Issue 9 (6th January 2009) Authors: Malan, V; Raoul, O; Firth, H V; Royer, G; Turleau, C; Bernheim, A; Willatt, L; Munnich, A; Vekemans, M; Lyonnet, S; Cormier-Daire, V; Colleaux, L Journal: Journal of medical genetics Issue: Volume 46:Issue 9(2009) Page Start: 635 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation. Issue 4 (1st August 2001) Authors: Marchio, A; Terris, B; Meddeb, M; Pineau, P; Duverger, A; Tiollais, P; Bernheim, A; Dejean, A Journal: Journal of clinical pathology Issue: Volume 54:Issue 4(2001) Page Start: 270 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH. (4th November 2012) Authors: Rio, M; Royer, G; Gobin, S; de, MC; Ozilou, C; Bernheim, A; Nizon, M; Munnich, A; Bonnefont, J‐P; Romana, S; Vekemans, M; Turleau, C; Malan, V Journal: Clinical genetics Issue: Volume 84:Number 1(2013:Jul.) Page Start: 31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗