Clinical spectrum of SIX3-associated mutations in holoprosencephaly: Correlation between genotype, phenotype and function

F. Lacbawan, B. D. Solomon, E. Roessler, K. El-Jaick, S. Domené, J. I. Vélez, N. Zhou, D. Hadley, J. Z. Balog, R. Long, A. Fryer, W. Smith, S. Omar, S. D. McLean, K. Clarkson, A. Lichty, N. J. Clegg, M. R. Delgado, E. Levey, E. StashinkoL. Potocki, M. I. VanAllen, J. Clayton-Smith, D. Donnai, D. W. Bianchi, P. B. Juliusson, P. R. Njølstad, H. G. Brunner, J. C. Carey, U. Hehr, J. Müsebeck, P. F. Wieacker, A. Postra, R. C.M. Hennekam, M. J.H. Van Den Boogaard, A. Van Haeringen, A. Paulussen, J. Herbergs, C. T.R.M. Schrander-Stumpel, A. R. Janecke, D. Chitayat, J. Hahn, D. M. McDonald-McGinn, E. H. Zackai, W. B. Dobyns, Maximilian Muenke

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