Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

C W Ockeloen; MH Willemsen; S de Munnik; BWM van Bon; N de Leeuw; A Verrips; SG Kant; EA Jones; HG Brunner; RLE Loon; EEJ Smeets; MM van Haelst; G van Haaften; A Nordgren; H Malmgren; G Grigelioniene; SE Vermeer; P Louro; L Ramos; T J J Maal; C C van Heumen; HG Yntema; CEL Carels; T Kleefstra

doi:10.1038/ejhg.2014.253

Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

C W Ockeloen
, MH Willemsen
, S de Munnik
, BWM van Bon
, N de Leeuw
, A Verrips
, SG Kant
, EA Jones
, HG Brunner
, RLE Loon
, EEJ Smeets
, MM van Haelst
, G van Haaften
, A Nordgren
, H Malmgren
, G Grigelioniene
, SE Vermeer
, P Louro
, L Ramos
, T J J Maal

C C van Heumen, HG Yntema, CEL Carels, T Kleefstra

Clinical Genetics

External organisation

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

91 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1176-1185
Number of pages	10
Journal	European Journal of Human Genetics
Volume	23
Issue number	9
DOIs	https://doi.org/10.1038/ejhg.2014.253
Publication status	Published - 2015

Research programs

EMC MGC-02-96-01

Access to Document

10.1038/ejhg.2014.253

Cite this

Ockeloen, C. W., Willemsen, MH., de Munnik, S., van Bon, BWM., de Leeuw, N., Verrips, A., Kant, SG., Jones, EA., Brunner, HG., Loon, RLE., Smeets, EEJ., van Haelst, MM., van Haaften, G., Nordgren, A., Malmgren, H., Grigelioniene, G., Vermeer, SE., Louro, P., Ramos, L., ... Kleefstra, T. (2015). Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations. European Journal of Human Genetics, 23(9), 1176-1185. https://doi.org/10.1038/ejhg.2014.253

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doi = "10.1038/ejhg.2014.253",

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Ockeloen, CW, Willemsen, MH, de Munnik, S, van Bon, BWM, de Leeuw, N, Verrips, A, Kant, SG, Jones, EA, Brunner, HG, Loon, RLE, Smeets, EEJ, van Haelst, MM, van Haaften, G, Nordgren, A, Malmgren, H, Grigelioniene, G, Vermeer, SE, Louro, P, Ramos, L, Maal, TJJ, van Heumen, CC, Yntema, HG, Carels, CEL & Kleefstra, T 2015, 'Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations', European Journal of Human Genetics, vol. 23, no. 9, pp. 1176-1185. https://doi.org/10.1038/ejhg.2014.253

TY - JOUR

T1 - Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

AU - Ockeloen, C W

AU - Willemsen, MH

AU - de Munnik, S

AU - van Bon, BWM

AU - de Leeuw, N

AU - Verrips, A

AU - Kant, SG

AU - Jones, EA

AU - Brunner, HG

AU - Loon, RLE

AU - Smeets, EEJ

AU - van Haelst, MM

AU - van Haaften, G

AU - Nordgren, A

AU - Malmgren, H

AU - Grigelioniene, G

AU - Vermeer, SE

AU - Louro, P

AU - Ramos, L

AU - Maal, T J J

AU - van Heumen, C C

AU - Yntema, HG

AU - Carels, CEL

AU - Kleefstra, T

PY - 2015

Y1 - 2015

U2 - 10.1038/ejhg.2014.253

DO - 10.1038/ejhg.2014.253

M3 - Article

C2 - 25424714

SN - 1018-4813

VL - 23

SP - 1176

EP - 1185

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -