Persistent URL of this record https://hdl.handle.net/1887/112975
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The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
- All authors
- Koolen, D.A.; Pfundt, R.; Linda, K.; Beunders, G.; Veenstra-Knol, H.E.; Conta, J.H.; Fortuna, A.M.; Gillessen-Kaesbach, G.; Dugan, S.; Halbach, S.; Abdul-Rahman, O.A.; Winesett, H.M.; Chung, W.K.; Dalton, M.; Dimova, P.S.; Mattina, T.; Prescott, K.; Zhang, H.Z.; Saal, H.M.; Hehir-Kwa, J.Y.; Willemsen, M.H.; Ockeloen, C.W.; Jongmans, M.C.; Aa, N. van der; Failla, P.; Barone, C.; Avola, E.; Brooks, A.S.; Kant, S.G.; Gerkes, E.H.; Firth, H.V.; Ounap, K.; Bird, L.M.; Masser-Frye, D.; Friedman, J.R.; Sokunbi, M.A.; Dixit, A.; Splitt, M.; Kukolich, M.K.; McGaughran, J.; Coe, B.P.; Florez, J.; Kasri, N.N.; Brunner, H.G.; Thompson, E.M.; Gecz, J.; Romano, C.; Eichler, E.E.; Vries, B.B.A. de; DDD Study
- Date
- 2016-05-31
- Volume
- 24
- Issue
- 5
- Pages
- 652 - 659