Authors: Kerr, AM Nomura, Y Armstrong, D Anvret, M Belichenko, PV Budden, S Cass, H Christodoulou, J Clarke, A Ellaway, C d'Esposito, M Francke, U Hulten, M Julu, P Leonard, H Naidu, S Schanen, C Webb, T Engerstrom, IW Yamashita, Y Segawa, M

Citation: Am. Kerr et al., Guidelines for reporting clinical features in cases with MECP2 mutations, BRAIN DEVEL, 23(4), 2001, pp. 208-211

Authors: Wan, MM Lee, SSJ Zhang, XY Houwink-Manville, I Song, HR Amir, RE Budden, S Naidu, S Pereira, JLP Lo, IFM Zoghbi, HY Schanen, NC Francke, U

Citation: Mm. Wan et al., Rett syndrome and beyond: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots, AM J HU GEN, 65(6), 1999, pp. 1520-1529