The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

Translated title of the contribution: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

B.W. van Bon, D.A. Koolen, L. Brueton, D. McMullan, X et al., K.D. Lichtenbelt, B.B. de Vries

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

Translated title of the contribution	The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
Original language	Undefined/Unknown
Pages (from-to)	163-170
Number of pages	8
Journal	European Journal of Human Genetics
Volume	18
Issue number	2
Publication status	Published - 2010

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title = "The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype",

author = "{van Bon}, B.W. and D.A. Koolen and L. Brueton and D. McMullan and {et al.}, X and K.D. Lichtenbelt and {de Vries}, B.B.",

year = "2010",

language = "Undefined/Unknown",

volume = "18",

pages = "163--170",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

number = "2",

}

TY - JOUR

T1 - The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

AU - van Bon, B.W.

AU - Koolen, D.A.

AU - Brueton, L.

AU - McMullan, D.

AU - et al., X

AU - Lichtenbelt, K.D.

AU - de Vries, B.B.

PY - 2010

Y1 - 2010

M3 - Article

SN - 1018-4813

VL - 18

SP - 163

EP - 170

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 2

ER -