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",

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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 -