1. Association study with two markers of a human homeogene in infantile autism. Issue 4 (April 1995) Authors: Petit, E; Hérault, J; Martineau, J; Perrot, A; Barthélémy, C; Hameury, L; Sauvage, D; Lelord, G; Müh, J P Journal: Journal of medical genetics Issue: Volume 32:Issue 4(1995) Page Start: 269 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and genetic characteristics of α cardiac actin gene mutations in hypertrophic cardiomyopathy. Issue 1 (16th January 2004) Authors: Mogensen, J; Perrot, A; Andersen, P S; Havndrup, O; Klausen, I C; Christiansen, M; Bross, P; Egeblad, H; Bundgaard, H; Osterziel, K J; Haltern, G; Lapp, H; Reinecke, P; Gregersen, N; Børglum, A D Journal: Journal of medical genetics Issue: Volume 41:Issue 1(2004) Page Start: e10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. P126The role of MIP1 in cardiac myocyte hypertrophy and survival. (15th July 2014) Authors: Mansfield, C; Buyandelger, B; Kostin, S; Knoell, G; Toliat, MR; Perrot, A; Haverkamp, W; Milting, H; Nurnberg, P; Knoell, R Journal: Cardiovascular research Issue: Volume 103(2014)Supplement 1 Page Start: S22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. We need a detailed phenome in the phenomenon of genetics and congenital heart disease. Issue 5 (28th April 2008) Authors: Posch, M G; Berger, F; Perrot, A; Özcelik, C Journal: Journal of medical genetics Issue: Volume 45:Issue 5(2008) Page Start: 320 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗