Further delineation of the KBG syndrome caused by ANKRD11 aberrations

Charlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik, Bregje W M van Bon, Nicole de Leeuw, Aad Verrips, Sarina G Kant, Elizabeth A Jones, Han G Brunner, Rosa L E van Loon, Eric E J Smeets, Mieke M van Haelst, Gijs van Haaften, Ann Nordgren, Helena Malmgren, Giedre Grigelioniene, Sascha Vermeer, Pedro Louro, Lina Ramos, Thomas J J MaalCeleste C van Heumen, Helger G Yntema, Carine E L Carels, Tjitske Kleefstra

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)1270
JournalEuropean Journal of Human Genetics
Volume23
Issue number9
DOIs
Publication statusPublished - Sep 2015

Cite this

Ockeloen, C. W., Willemsen, M. H., de Munnik, S., van Bon, B. W. M., de Leeuw, N., Verrips, A., ... Kleefstra, T. (2015). Further delineation of the KBG syndrome caused by ANKRD11 aberrations. European Journal of Human Genetics, 23(9), 1270. https://doi.org/10.1038/ejhg.2015.130