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

doi:https://doi.org/10.1038/ejhg.2012.57

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

Human Genetics (VUmc)

Research output: Contribution to journal › Article › Academic › peer-review

35 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1024-1031
Journal	European journal of human genetics
Volume	20
Issue number	10
DOIs	https://doi.org/10.1038/ejhg.2012.57
Publication status	Published - 2012

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https://doi.org/10.1038/ejhg.2012.57

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

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Mansour, S, Swinkels, M, Terhal, PA, Wilson, LC, Rich, P, van Maldergem, L, Zwijnenburg, PJG, Hall, CM, Robertson, SP & Newbury-Ecob, R 2012, 'Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance', European journal of human genetics, vol. 20, no. 10, pp. 1024-1031. https://doi.org/10.1038/ejhg.2012.57

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AU - Swinkels, M.

AU - Terhal, P.A.

AU - Wilson, L.C.

AU - Rich, P.

AU - van Maldergem, L.

AU - Zwijnenburg, P.J.G.

AU - Hall, C.M.

AU - Robertson, S.P.

AU - Newbury-Ecob, R.

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