Correction

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, Miho Adachi-Fukuda, Yasemin Alanay, Adila AlKindy, Anwar Baban, Allan Bayat, Stefanie Beck-Wödl, Katherine Berry, Emilia K Bijlsma, Levinus A Bok, Alwin F J Brouwer, Ineke van der Burgt, Philippe M Campeau, Natalie Canham, Krystyna Chrzanowska, Yoyo W Y Chu, Brain H Y Chung, Karin Dahan & 85 others Marjan De Rademaeker, Anne Destree, Tracy Dudding-Byth, Rachel Earl, Nursel Elcioglu, Ellen R Elias, Christina Fagerberg, Alice Gardham, Blanca Gener, Erica H Gerkes, Ute Grasshoff, Arie van Haeringen, Karin R Heitink, Johanna C Herkert, Nicolette S den Hollander, Denise Horn, David Hunt, Sarina G Kant, Mitsuhiro Kato, Hülya Kayserili, Rogier Kersseboom, Esra Kilic, Malgorzata Krajewska-Walasek, Kylin Lammers, Lone W Laulund, Damien Lederer, Melissa Lees, Vanesa López-González, Saskia Maas, Grazia M S Mancini, Carlo Marcelis, Francisco Martinez, Isabelle Maystadt, Marianne McGuire, Shane McKee, Sarju Mehta, Kay Metcalfe, Jeff Milunsky, Seiji Mizuno, John B Moeschler, Christian Netzer, Charlotte W Ockeloen, Barbara Oehl-Jaschkowitz, Nobuhiko Okamoto, Sharon N M Olminkhof, Carmen Orellana, Laurent Pasquier, Caroline Pottinger, Vera Riehmer, Stephen P Robertson, Maian Roifman, Caroline Rooryck, Fabienne G Ropers, Monica Rosello, Claudia A L Ruivenkamp, Mahmut S Sagiroglu, Suzanne C E H Sallevelt, Amparo Sanchis Calvo, Pelin O Simsek-Kiper, Gabriela Soares, Lucia Solaeche, Fatma Mujgan Sonmez, Miranda Splitt, Duco Steenbeek, Alexander P A Stegmann, Constance T R M Stumpel, Saori Tanabe, Eyyup Uctepe, G Eda Utine, Hermine E Veenstra-Knol, Sunita Venkateswaran, Catheline Vilain, Catherine Vincent-Delorme, Anneke T Vulto-van Silfhout, Patricia Wheeler, Golder N Wilson, Louise C Wilson, Bernd Wollnik, Tomoki Kosho, Dagmar Wieczorek, Evan Eichler, Rolph Pfundt, Bert B A de Vries, Jill Clayton-Smith, Gijs W E Santen

Research output: Contribution to journalArticle

Abstract

The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Article.

Original languageEnglish
JournalGenetics in Medicine
DOIs
Publication statusE-pub ahead of print - Jan 29 2019

Fingerprint

Intellectual Disability
Coffin-Siris syndrome

Cite this

van der Sluijs, P. J., Jansen, S., Vergano, S. A., Adachi-Fukuda, M., Alanay, Y., AlKindy, A., ... Santen, G. W. E. (2019). Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. Genetics in Medicine. https://doi.org/10.1038/s41436-018-0368-y

Correction : The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. / 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; 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, 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; 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.

In: Genetics in Medicine, 29.01.2019.

Research output: Contribution to journalArticle

van der Sluijs, PJ, Jansen, S, Vergano, SA, Adachi-Fukuda, M, Alanay, Y, AlKindy, A, Baban, A, Bayat, A, Beck-Wödl, S, Berry, K, Bijlsma, EK, Bok, LA, Brouwer, AFJ, van der Burgt, I, Campeau, PM, Canham, N, Chrzanowska, K, Chu, YWY, Chung, BHY, Dahan, K, De Rademaeker, M, Destree, A, Dudding-Byth, T, Earl, R, Elcioglu, N, Elias, ER, Fagerberg, C, Gardham, A, Gener, B, Gerkes, EH, Grasshoff, U, van Haeringen, A, Heitink, KR, Herkert, JC, den Hollander, NS, Horn, D, Hunt, D, Kant, SG, Kato, M, Kayserili, H, Kersseboom, R, Kilic, E, Krajewska-Walasek, M, Lammers, K, Laulund, LW, Lederer, D, Lees, M, López-González, V, Maas, S, Mancini, GMS, Marcelis, C, Martinez, F, Maystadt, I, McGuire, M, McKee, S, Mehta, S, Metcalfe, K, Milunsky, J, Mizuno, S, Moeschler, JB, Netzer, C, Ockeloen, CW, Oehl-Jaschkowitz, B, Okamoto, N, Olminkhof, SNM, Orellana, C, Pasquier, L, Pottinger, C, Riehmer, V, Robertson, SP, Roifman, M, Rooryck, C, Ropers, FG, Rosello, M, Ruivenkamp, CAL, Sagiroglu, MS, Sallevelt, SCEH, Calvo, AS, Simsek-Kiper, PO, Soares, G, Solaeche, L, Sonmez, FM, Splitt, M, Steenbeek, D, Stegmann, APA, Stumpel, CTRM, Tanabe, S, Uctepe, E, Utine, GE, Veenstra-Knol, HE, Venkateswaran, S, Vilain, C, Vincent-Delorme, C, Vulto-van Silfhout, AT, Wheeler, P, Wilson, GN, Wilson, LC, Wollnik, B, Kosho, T, Wieczorek, D, Eichler, E, Pfundt, R, de Vries, BBA, Clayton-Smith, J & Santen, GWE 2019, 'Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome', Genetics in Medicine. https://doi.org/10.1038/s41436-018-0368-y
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 ; 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, 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 ; 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. / Correction : The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. In: Genetics in Medicine. 2019.
@article{f5b3f4816d58447aac2d0e96e8609de8,
title = "Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome",
abstract = "The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Article.",
author = "{van der Sluijs}, {Pleuntje J} and Sandra Jansen and Vergano, {Samantha A} and Miho Adachi-Fukuda and Yasemin Alanay and Adila AlKindy and Anwar Baban and Allan Bayat and Stefanie Beck-W{\"o}dl and Katherine Berry and Bijlsma, {Emilia K} and Bok, {Levinus A} and Brouwer, {Alwin F J} and {van der Burgt}, Ineke and Campeau, {Philippe M} and Natalie Canham and Krystyna Chrzanowska and Chu, {Yoyo W Y} and Chung, {Brain H Y} and Karin Dahan and {De Rademaeker}, Marjan and Anne Destree and Tracy Dudding-Byth and Rachel Earl and Nursel Elcioglu and Elias, {Ellen R} and Christina Fagerberg and Alice Gardham and Blanca Gener and Gerkes, {Erica H} and Ute Grasshoff and {van Haeringen}, Arie and Heitink, {Karin R} and Herkert, {Johanna C} and {den Hollander}, {Nicolette S} and Denise Horn and David Hunt and Kant, {Sarina G} and Mitsuhiro Kato and H{\"u}lya Kayserili and Rogier Kersseboom and Esra Kilic and Malgorzata Krajewska-Walasek and Kylin Lammers and Laulund, {Lone W} and Damien Lederer and Melissa Lees and Vanesa L{\'o}pez-Gonz{\'a}lez and Saskia Maas and Mancini, {Grazia M S} and Carlo Marcelis and Francisco Martinez and Isabelle Maystadt and Marianne McGuire and Shane McKee and Sarju Mehta and Kay Metcalfe and Jeff Milunsky and Seiji Mizuno and Moeschler, {John B} and Christian Netzer and Ockeloen, {Charlotte W} and Barbara Oehl-Jaschkowitz and Nobuhiko Okamoto and Olminkhof, {Sharon N M} and Carmen Orellana and Laurent Pasquier and Caroline Pottinger and Vera Riehmer and Robertson, {Stephen P} and Maian Roifman and Caroline Rooryck and Ropers, {Fabienne G} and Monica Rosello and Ruivenkamp, {Claudia A L} and Sagiroglu, {Mahmut S} and Sallevelt, {Suzanne C E H} and Calvo, {Amparo Sanchis} and Simsek-Kiper, {Pelin O} and Gabriela Soares and Lucia Solaeche and Sonmez, {Fatma Mujgan} and Miranda Splitt and Duco Steenbeek and Stegmann, {Alexander P A} and Stumpel, {Constance T R M} and Saori Tanabe and Eyyup Uctepe and Utine, {G Eda} and Veenstra-Knol, {Hermine E} and Sunita Venkateswaran and Catheline Vilain and Catherine Vincent-Delorme and {Vulto-van Silfhout}, {Anneke T} and Patricia Wheeler and Wilson, {Golder N} and Wilson, {Louise C} and Bernd Wollnik and Tomoki Kosho and Dagmar Wieczorek and Evan Eichler and Rolph Pfundt and {de Vries}, {Bert B A} and Jill Clayton-Smith and Santen, {Gijs W E}",
year = "2019",
month = "1",
day = "29",
doi = "10.1038/s41436-018-0368-y",
language = "English",
journal = "Genetics in Medicine",
issn = "1098-3600",
publisher = "Nature Publishing Group",

}

TY - JOUR

T1 - Correction

T2 - The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

AU - van der Sluijs, Pleuntje J

AU - Jansen, Sandra

AU - Vergano, Samantha A

AU - Adachi-Fukuda, Miho

AU - Alanay, Yasemin

AU - AlKindy, Adila

AU - Baban, Anwar

AU - Bayat, Allan

AU - Beck-Wödl, Stefanie

AU - Berry, Katherine

AU - Bijlsma, Emilia K

AU - Bok, Levinus A

AU - Brouwer, Alwin F J

AU - van der Burgt, Ineke

AU - Campeau, Philippe M

AU - Canham, Natalie

AU - Chrzanowska, Krystyna

AU - Chu, Yoyo W Y

AU - Chung, Brain H Y

AU - Dahan, Karin

AU - De Rademaeker, Marjan

AU - Destree, Anne

AU - Dudding-Byth, Tracy

AU - Earl, Rachel

AU - Elcioglu, Nursel

AU - Elias, Ellen R

AU - Fagerberg, Christina

AU - Gardham, Alice

AU - Gener, Blanca

AU - Gerkes, Erica H

AU - Grasshoff, Ute

AU - van Haeringen, Arie

AU - Heitink, Karin R

AU - Herkert, Johanna C

AU - den Hollander, Nicolette S

AU - Horn, Denise

AU - Hunt, David

AU - Kant, Sarina G

AU - Kato, Mitsuhiro

AU - Kayserili, Hülya

AU - Kersseboom, Rogier

AU - Kilic, Esra

AU - Krajewska-Walasek, Malgorzata

AU - Lammers, Kylin

AU - Laulund, Lone W

AU - Lederer, Damien

AU - Lees, Melissa

AU - López-González, Vanesa

AU - Maas, Saskia

AU - Mancini, Grazia M S

AU - Marcelis, Carlo

AU - Martinez, Francisco

AU - Maystadt, Isabelle

AU - McGuire, Marianne

AU - McKee, Shane

AU - Mehta, Sarju

AU - Metcalfe, Kay

AU - Milunsky, Jeff

AU - Mizuno, Seiji

AU - Moeschler, John B

AU - Netzer, Christian

AU - Ockeloen, Charlotte W

AU - Oehl-Jaschkowitz, Barbara

AU - Okamoto, Nobuhiko

AU - Olminkhof, Sharon N M

AU - Orellana, Carmen

AU - Pasquier, Laurent

AU - Pottinger, Caroline

AU - Riehmer, Vera

AU - Robertson, Stephen P

AU - Roifman, Maian

AU - Rooryck, Caroline

AU - Ropers, Fabienne G

AU - Rosello, Monica

AU - Ruivenkamp, Claudia A L

AU - Sagiroglu, Mahmut S

AU - Sallevelt, Suzanne C E H

AU - Calvo, Amparo Sanchis

AU - Simsek-Kiper, Pelin O

AU - Soares, Gabriela

AU - Solaeche, Lucia

AU - Sonmez, Fatma Mujgan

AU - Splitt, Miranda

AU - Steenbeek, Duco

AU - Stegmann, Alexander P A

AU - Stumpel, Constance T R M

AU - Tanabe, Saori

AU - Uctepe, Eyyup

AU - Utine, G Eda

AU - Veenstra-Knol, Hermine E

AU - Venkateswaran, Sunita

AU - Vilain, Catheline

AU - Vincent-Delorme, Catherine

AU - Vulto-van Silfhout, Anneke T

AU - Wheeler, Patricia

AU - Wilson, Golder N

AU - Wilson, Louise C

AU - Wollnik, Bernd

AU - Kosho, Tomoki

AU - Wieczorek, Dagmar

AU - Eichler, Evan

AU - Pfundt, Rolph

AU - de Vries, Bert B A

AU - Clayton-Smith, Jill

AU - Santen, Gijs W E

PY - 2019/1/29

Y1 - 2019/1/29

N2 - The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Article.

AB - The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Article.

U2 - 10.1038/s41436-018-0368-y

DO - 10.1038/s41436-018-0368-y

M3 - Article

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

ER -