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    The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome von van der Sluijs, Pleuntje J., Jansen, Sandra, Vergano, Samantha A., Adachi-Fukuda, Miho, Alanay, Yasemin, AlKindy, Adila, Baban, Anwar, Bayat, Allan, Beck-Wödl, Stefanie, Berry, Katherine, Bijlsma, Emilia K., Bok, Levinus A., Brouwer, Alwin F. J., van der Burgt, Ineke, Campeau, Philippe M., Canham, Natalie, Chrzanowska, Krystyna, 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, Hülya, 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, Martinez, Francisco, Maystadt, Isabelle, McGuire, Marianne, McKee, Shane, Mehta, Sarju, Metcalfe, Kay, 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, Monica, Ruivenkamp, Claudia A. L., Sagiroglu, Mahmut S., Sallevelt, Suzanne C. E. H., Sanchis Calvo, Amparo, Simsek-Kiper, Pelin O., Soares, Gabriela, Solaeche, Lucia, 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, 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., Santen, Gijs W. E.

    Veröffentlicht in Genetics in medicine

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    Correction: The ARID1B spectrum in 143 patients: fromnonsyndromic intellectual disability to Coffin–Siris syndrome von Jansen, Sandra, Vergano Samantha A, Adachi-Fukuda Miho, Alanay Yasemin, AlKindy Adila, Baban Anwar, Bayat, Allan, Beck-Wödl 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, 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, Kato Mitsuhiro, Kayserili Hülya, Kersseboom Rogier, Kilic Esra, Krajewska-Walasek Malgorzata, Lammers Kylin, Laulund, Lone W, Lederer, Damien, Lees, Melissa, López-González Vanesa, Maas Saskia, Mancini, Grazia M, Marcelis, Carlo, Martinez, 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, Pasquier, Laurent, Pottinger, Caroline, Riehmer Vera, Robertson, Stephen P, Roifman Maian, Rooryck Caroline, Ropers, Fabienne G, Rosello, Monica, Ruivenkamp Claudia A L, Sagiroglu, Mahmut S, Sallevelt Suzanne C E H, Calvo, Amparo Sanchis, Simsek-Kiper, Pelin O, Soares, Gabriela, Solaeche Lucia, Sonmez Fatma Mujgan, Splitt Miranda, Steenbeek Duco, Stegmann Alexander P A, Stumpel Constance T R M, Tanabe Saori, Eyyup, Uctepe, Eda, Utine G, Veenstra-Knol, Hermine E, Venkateswaran Sunita, Vilain Catheline, Vincent-Delorme, Catherine, Wheeler, Patricia, Wilson, Golder N, Wilson, Louise C, Wollnik Bernd, Kosho Tomoki, Wieczorek Dagmar, Eichler, Evan, Rolph, Pfundt, de Vries Bert B A, Clayton-Smith, Jill, Santen Gijs W E

    Veröffentlicht in Genetics in medicine

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    Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome von van der Sluijs, Pleuntje J., Jansen, Sandra, Vergano, Samantha A., Alanay, Yasemin, AlKindy, Adila, Baban, Anwar, Bayat, Allan, Beck-Wödl, Stefanie, Berry, Katherine, Bijlsma, Emilia K., Brouwer, Alwin F.J., van der Burgt, Ineke, Campeau, Philippe M., Canham, Natalie, Chrzanowska, Krystyna, 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, 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, Hülya, 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, Martinez, 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, Monica, Ruivenkamp, Claudia A.L., Sagiroglu, Mahmut S., Sallevelt, Suzanne C.E.H., Calvo, Amparo Sanchis, Simsek-Kiper, Pelin O., Soares, Gabriela, Solaeche, Lucia, 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.

    Veröffentlicht in Genetics in medicine

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