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

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

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

Translated title of the contribution: Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance

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

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

Translated title of the contribution	Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance
Original language	Undefined/Unknown
Pages (from-to)	1024-1031
Number of pages	8
Journal	European Journal of Human Genetics
Volume	20
Issue number	10
Publication status	Published - 2012

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/22473091

Cite this

Mansour, S., Swinkels, M. E. M., Terhal, P. A., Wilson, L. C., Rich, P., van Maldergem, L., Zwijnenburg, P. J., 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. http://www.ncbi.nlm.nih.gov/pubmed/22473091

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title = "Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance",

author = "S. Mansour and M.E.M. Swinkels and P.A. Terhal and L.C. Wilson and P. Rich and {van Maldergem}, L. and P.J. Zwijnenburg and C.M. Hall and S.P. Robertson and R. Newbury-Ecob",

year = "2012",

language = "Undefined/Unknown",

volume = "20",

pages = "1024--1031",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

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Mansour, S, Swinkels, MEM, Terhal, PA, Wilson, LC, Rich, P, van Maldergem, L, Zwijnenburg, PJ, 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. <http://www.ncbi.nlm.nih.gov/pubmed/22473091>

TY - JOUR

T1 - Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance

AU - Mansour, S.

AU - Swinkels, M.E.M.

AU - Terhal, P.A.

AU - Wilson, L.C.

AU - Rich, P.

AU - van Maldergem, L.

AU - Zwijnenburg, P.J.

AU - Hall, C.M.

AU - Robertson, S.P.

AU - Newbury-Ecob, R.

PY - 2012

Y1 - 2012

M3 - Article

SN - 1018-4813

VL - 20

SP - 1024

EP - 1031

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 10

ER -