학술논문
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
Document Type
Artikel
Author
Ockeloen, CW; Willemsen, MH; de Munnik, S; van Bon, BWM; de Leeuw, N; Verrips, A; Kant, SG; Jones, EA; Brunner, HG; van Loon, RLE; Smeets, EEJ; van Haelst, MM; van Haaften, G; Nordgren, A; Malmgren, H; Grigelioniene, G; Vermeer, S; Louro, P; Ramos, L; Maal, TJJ; van Heumen, CC; Yntema, HG; Carels, CEL; Kleefstra, T
Source
European journal of human genetics : EJHG. 23(9):1176-1185
Subject
Language
English
English
English
ISSN
1476-5438