YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
- Author(s):
- Gabriele, M.; Vulto-van Silfhout, A.T.; Germain, P.L.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.R.J.; Stromme, P.; Rosenfeld, J.A.; Shao, Y.R.; Craigen, W.J.; Schaaf, C.P.; Rodriguez-Buritica, D.; Farach, L.; Friedman, J.; Thulin, P.; McLean, S.D.; Nugent, K.M.; Morton, J.; Nicholl, J.; Andrieux, J.; Stray-Pedersen, A.; Chambon, P.; Patrier, S.; Lynch, S.A.; Kjaergaard, S.; Torring, P.M.; Brasch-Andersen, C.; Ronan, A.; Haeringen, A. van (0000-0003-3786-6716); Anderson, P.J.; Powis, Z.; Brunner, H.G.; Pfundt, R.; Schuurs-Hoeijmakers, J.H.M.; Bon, B.W.M. van; Lelieveld, S.; Gilissen, C.; Nillesen, W.M.; Vissers, L.E.L.M.; Gecz, J.; Koolen, D.A.; Testa, G.; Vries, B.B.A. de
- Published
- 2017
- Publication type
- Article / Letter to editor
- Date issued
- 2017-06-01
- Language
- English
- Is part of
- American Journal of Human Genetics (2017), Vol. 100, no. 6, p. 907-925
- hdl
- 1887/94674
- doi
- 10.1016/j.ajhg.2017.05.006
