Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype

✍ Scribed by Kleefstra, T; van Zelst-Stams, W A; Nillesen, W M; Cormier-Daire, V; Houge, G; Foulds, N; van Dooren, M; Willemsen, M H; Pfundt, R; Turner, A; Wilson, M; McGaughran, J; Rauch, A; Zenker, M; Adam, M P; Innes, M; Davies, C; Lopez, A G.-M.; Casalone, R; Weber, A; Brueton, L A; Navarro, A D.; Bralo, M P.; Venselaar, H; Stegmann, S P A; Yntema, H G; van Bokhoven, H; Brunner, H G

• Book ID: 124078395
• Publisher: BMJ Publishing Group
• Year: 2009
• Tongue: English
• Weight: 797 KB
• Volume: 46
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.2008.062950