van-der-Sluijs, Pleuntje-J; Jansen, Sandra; Vergano, Samantha-A; Adachi-Fukuda, Miho; Alanay, Yasemin; AlKindy, Adila; Baban, Anwar; Bayat, Allan; Beck-Woedl, Stefanie; Berry, Katherine; Bijlsma, Emilia-K; Bok, Levinus-A; Brouwer, Alwin-F-J; van-der-Burgt, Ineke; Campeau, Philippe-M; Canham, Natalie; Chrzanowska, Krystyna; Chu, Yoyo-W-Y; Chung, Brain-H-Y; Dahan, Karin; De-Rademaeker, Marjan; Destree, Anne; Dudding-Byth, Tracy; Earl, Rachel; Elcioglu, Nursel; Elias, Ellen-R; Fagerberg, Christina; Gardham, Alice; Gener, Blanca; Gerkes, Erica-H; Grasshoff, Ute; van-Haeringen, Arie; Heitink, Karin-R; Herkert, Johanna-C; den-Hollander, Nicolette-S; Horn, Denise; Hunt, David; Kant, Sarina-G; Kato, Mitsuhiro; Kayserili, Hulya; Kersseboom, Rogier; Kilic, Esra; Krajewska-Walasek, Malgorzata; Lammers, Kylin; Laulund, Lone-W; Lederer, Damien; Lees, Melissa; López-González, Vanesa; Maas, Saskia; Mancini, Grazia-M-S; Marcelis, Carlo; Martínez, Francisco; Maystadt, Isabelle; McGuire, Marianne; McKee, Shane; Mehta, Sarju; Metcalfe, Kay; Milunsky, Jeff; Mizuno, Seiji; Moeschler, John-B; Netzer, Christian; Ockeloen, Charlotte-W; Oehl-Jaschkowitz, Barbara; Okamoto, Nobuhiko; Olminkhof, Sharon-N-M; Orellana, Carmen; Pasquier, Laurent; Pottinger, Caroline; Riehmer, Vera; Robertson, Stephen-P; Roifman, Maian; Rooryck, Caroline; Ropers, Fabienne-G; Rosello, Mónica; Ruivenkamp, Claudia-A-L; Sagiroglu, Mahmut-S; Sallevelt, Suzanne-C-E-H; Sanchis-Calvo, Amparo; Simsek-Kiper, Pelin-O; Soares, Gabriela; Solaeche, Lucía; Sonmez, Fatma-Mujgan; Splitt, Miranda; Steenbeek, Duco; Stegmann, Alexander-P-A; Stumpel, Constance-T-R-M; Tanabe, Saori; Uctepe, Eyyup; Utine, G-Eda; Veenstra-Knol, Hermine-E; Venkateswaran, Sunita; Vilain, Catheline; Vincent-Delorme, Catherine; Vulto-van-Silfhout, Anneke-T; Wheeler, Patricia; Wilson, Golder-N; Wilson, Louise-C; Wollnik, Bernd; Kosho, Tomoki; Wieczorek, Dagmar; Eichler, Evan; Pfundt, Rolph; de-Vries, Bert-B-A; Clayton-Smith, Jill; Santen, Gijs-W-E
(SPRINGERNATURE, 2019-06)
PURPOSE: Pathogenic variants in ARID1B are one of the most frequent causes of intellectual disability (ID) as determined by large-scale exome sequencing studies. Most studies published thus far describe clinically diagnosed ...