The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes

A.D.C. Paulussen, C.T. Schrander-Stumpel, D.C.J. Tserpelis, M.K.M. Spee, A.P.A. Stegmann, G.M. Mancini, A.S. Brooks, M. Collee, A. Maat-Kievit, M.E.H. Simon, Y. van Bever, I. Stolte-Dijkstra, W.S. Kerstjens-Frederikse, J.C. Herkert, A.J. van Essen, K.D. Lichtenbelt, A. van Haeringen, M.L. Kwee, A.M.A. Lachmeijer, M.B. SindhunataM.C. van Maarle, Y.H.J.M. Arens, E.E.J.G. Smeets, C.E. de Die-Smulders, J.J.M. Engelen, H.J. Smeets, J. Herbergs

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)999-1005
JournalEuropean Journal of Human Genetics
Volume18
Issue number9
DOIs
Publication statusPublished - 2010

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Paulussen, A. D. C., Schrander-Stumpel, C. T., Tserpelis, D. C. J., Spee, M. K. M., Stegmann, A. P. A., Mancini, G. M., ... Herbergs, J. (2010). The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes. European Journal of Human Genetics, 18(9), 999-1005. https://doi.org/10.1038/ejhg.2010.70