Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

Ockeloen, CW (author)

Willemsen, MH (author)

de Munnik, S (author)

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van Bon, BWM (author)

de Leeuw, N (author)

Verrips, A (author)

Kant, SG (author)

Jones, EA (author)

Brunner, HG (author)

van Loon, RLE (author)

Smeets, EEJ (author)

van Haelst, MM (author)

van Haaften, G (author)

Nordgren, A (author)

Karolinska Institutet

Malmgren, H (author)

Karolinska Institutet

Grigelioniene, G (author)

Karolinska Institutet

Vermeer, S (author)

Louro, P (author)

Ramos, L (author)

Maal, TJJ (author)

van Heumen, CC (author)

Yntema, HG (author)

Carels, CEL (author)

Kleefstra, T (author)

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 (creator_code:org_t)

2014-11-26

2015

English.

In: European journal of human genetics : EJHG. - : Springer Science and Business Media LLC. - 1476-5438 .- 1018-4813. ; 23:9, s. 1176-1185

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• Journal article (peer-reviewed)