Further delineation of the KBG syndrome caused by ANKRD11 aberrations.
Ockeloen CW, Willemsen MH, de Munnik S, van Bon BW, de Leeuw N, Verrips A, Kant SG, Jones EA, Brunner HG, van Loon RL, Smeets EE, van Haelst MM, van Haaften G, Nordgren A, Malmgren H, Grigelioniene G, Vermeer S, Louro P, Ramos L, Maal TJ, van Heumen CC, Yntema HG, Carels CE, Kleefstra T.
Ockeloen CW, et al. Among authors: maal tj.
Eur J Hum Genet. 2015 Sep;23(9):1270. doi: 10.1038/ejhg.2015.130.
Eur J Hum Genet. 2015.
PMID: 26269249
Free PMC article.
No abstract available.