van der Sluijs, Pleuntje J.Jansen, SandraVergano, Samantha A.Adachi-Fukuda, MihoAlanay, YaseminAlKindy, AdilaBaban, AnwarBayat, AllanBeck-Woedl, StefanieBerry, KatherineBijlsma, Emilia K.Bok, Levinus A.Brouwer, Alwin F. J.van der Burgt, InekeCampeau, Philippe M.Canham, NatalieChrzanowska, KrystynaChu, Yoyo W. Y.Chung, Brain H. Y.Dahan, KarinDe Rademaeker, MarjanDestree, AnneDudding-Byth, TracyEarl, RachelElcioglu, NurselElias, Ellen R.Fagerberg, ChristinaGardham, AliceGener, BlancaGerkes, Erica H.Grasshoff, Utevan Haeringen, ArieHeitink, Karin R.Herkert, Johanna C.den Hollander, Nicolette S.Horn, DeniseHunt, DavidKant, Sarina G.Kato, MitsuhiroKayserili, HulyaKersseboom, RogierKilic, EsraKrajewska-Walasek, MalgorzataLammers, KylinLaulund, Lone W.Lederer, DamienLees, MelissaLopez-Gonzalez, VanesaMaas, SaskiaMancini, Grazia M. S.Marcelis, CarloMartinez, FranciscoMaystadt, IsabelleMcGuire, MarianneMckee, ShaneMehta, SarjuMetcalfe, KayMilunsky, JeffMizuno, SeijiMoeschler, John B.Netzer, ChristianOckeloen, Charlotte W.Oehl-Jaschkowitz, BarbaraOkamoto, NobuhikoOlminkhof, Sharon N. M.Orellana, CarmenPasquier, LaurentPottinger, CarolineRiehmer, VeraRobertson, Stephen P.Roifman, MaianRooryck, CarolineRopers, Fabienne G.Rosello, MonicaRuivenkamp, Claudia A. L.Sagiroglu, Mahmut S.Sallevelt, Suzanne C. E. H.Calvo, Amparo SanchisSimsek-Kiper, Pelin O.Soares, GabrielaSolaeche, LuciaSonmez, Fatma MujganSplitt, MirandaSteenbeek, DucoStegmann, Alexander P. A.Stumpel, Constance T. R. M.Tanabe, SaoriUctepe, EyyupUtine, G. EdaVeenstra-Knol, Hermine E.Venkateswaran, SunitaVilain, CathelineVincent-Delorme, CatherineVulto-van Silfhout, Anneke T.Wheeler, PatriciaWilson, Golder N.Wilson, Louise C.Wollnik, BerndKosho, TomokiWieczorek, DagmarEichler, EvanPfundt, Rolphde Vries, Bert B. A.Clayton-Smith, JillSanten, Gijs W. E.2023-02-212023-02-212019-01-0110.1038/s41436-018-0368-yhttps://hdl.handle.net/11443/2885http://dx.doi.org/10.1038/s41436-018-0368-yThe ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome (vol 21, pg 1295, 2019)ArticleWOS:000484400800031