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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2015 Aug 13;23(9):1270. doi: 10.1038/ejhg.2015.130

Further delineation of the KBG syndrome caused by ANKRD11 aberrations

Charlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik, Bregje WM van Bon, Nicole de Leeuw, Aad Verrips, Sarina G Kant, Elizabeth A Jones, Han G Brunner, Rosa LE van Loon, Eric EJ Smeets, Mieke M van Haelst, Gijs van Haaften, Ann Nordgren, Helena Malmgren, Giedre Grigelioniene, Sascha Vermeer, Pedro Louro, Lina Ramos, Thomas JJ Maal, Celeste C van Heumen, Helger G Yntema, Carine EL Carels, Tjitske Kleefstra
PMCID: PMC4538192  PMID: 26269249

Correction to: European Journal of Human Genetics advance online publication, 26 November 2014; doi:10.1038/ejhg.2014.253

Since the publication of this article, the authors have noted that the coordinates and size of the microdeletion in patient 13 were not mentioned correctly throughout the article. This issue has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified.

The authors would like to apologise for their oversight.


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