Einträge von Clegg, N J auf dem Publikationsserver

Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K , Domene, S, Velez, J I , Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njolstad, P R, Brunner, H G, Carey, J C, Hehr, U, Musebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R , Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B und Muenke, M (2009) Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. Journal of Medical Genetics 46 (6), S. 389-398. Volltext nicht vorhanden.