Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance

S. Mansour, M. Swinkels, P.A. Terhal, L.C. Wilson, P. Rich, L. van Maldergem, P.J.G. Zwijnenburg, C.M. Hall, S.P. Robertson, R. Newbury-Ecob

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1024-1031
JournalEuropean Journal of Human Genetics
Volume20
Issue number10
DOIs
Publication statusPublished - 2012

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Mansour, S., Swinkels, M., Terhal, P. A., Wilson, L. C., Rich, P., van Maldergem, L., ... Newbury-Ecob, R. (2012). Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance. European Journal of Human Genetics, 20(10), 1024-1031. https://doi.org/10.1038/ejhg.2012.57