Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

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; 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; H. lya 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

doi:https://doi.org/10.1038/s41436-018-0368-y

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

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 DahanMarjan 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, H. lya 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 journal › Comment/Letter to the editor › Academic

4 Citations (Scopus)

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 language	English
Pages (from-to)	2160-2161
Number of pages	2
Journal	Genetics in medicine
Volume	21
Issue number	9
Early online date	29 Jan 2019
DOIs	https://doi.org/10.1038/s41436-018-0368-y
Publication status	Published - 1 Sept 2019

Access to Document

https://doi.org/10.1038/s41436-018-0368-y

Cite this

van der Sluijs, P. J., Jansen, S., Vergano, S. A., Adachi-Fukuda, M., Alanay, Y., AlKindy, A., Baban, A., Bayat, A., Beck-Wödl, S., Berry, K., Bijlsma, E. K., Bok, L. A., Brouwer, A. F. J., van der Burgt, I., Campeau, P. M., Canham, N., Chrzanowska, K., Chu, Y. W. Y., Chung, B. H. Y., ... Santen, G. W. E. (2019). Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z). Genetics in medicine, 21(9), 2160-2161. https://doi.org/10.1038/s41436-018-0368-y

@article{c5ba1351164143d48811769002093119,

title = "Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)",

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 Kayserili, {H. lya} 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.}",

note = "Funding Information: and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China; 19Center for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium; 20Center for Medical Genetics, Vrije Universiteit Brussels, Brussels, Belgium; 21Hunter Genetics and University of Newcastle, GrowUpWell Priority Research Centre, Newcastle, Australia; 22Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA; 23Department of Pediatric Genetics, Marmara University Pendik Hospital, Istanbul, Turkey; 24Department of Pediatrics and Genetics, University of Colorado Denver School of Medicine, Aurora, CO, USA; 25Department of Clinical Genetics, Odense University Hospital, Odense, Denmark; 26Department of Genetics, Cruces University Hospital, Biocruces Health Research Institute, Vizcayam, Spain; 27University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands; 28Department of Rehabilitation Medicine, Leiden University Medical Center, Leiden, The Netherlands; 29Institute for Medical Genetics and Human Genetics, Charit{\'e} Universit{\"a}tsmedizin, Berlin, Germany; 30Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom; 31Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan; 32Medical Genetics Department, Ko{\c c} University School of Medicine (KUSoM), İstanbul, Turkey; 33Department of Clinical Genetics, Sophia Children{\textquoteright}s Hospital, Erasmus MC, Rotterdam, The Netherlands; 34Department of Pediatric Genetics, Hematology Oncology Research & Training Children{\textquoteright}s Hospital, Ankara, Turkey; 35Department of Medical Genetics, Dayton Children{\textquoteright}s Hospital, Dayton, OH, USA; 36Department of Paediatrics, Odense University Hospital, Odense, Denmark; 37Department of Clinical Genetics, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom; 38Secci{\'o}n de Gen{\'e}tica M{\'e}dica, Servicio de Pediatria, Hospital Clinico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, CIBERERISCIII, Murcia, Spain; 39Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; 40Unidad de Gen{\'e}tica, Hospital Universitario y Polit{\'e}cnico La Fe, Valencia, Spain; 41Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA; 42Northern Ireland Regional Genetics Centre, Belfast City Hospital, Belfast, Ireland; 43East Anglian Regional Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke{\textquoteright}s Hospital, Cambridge, United Kingdom; 44Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, St Mary{\textquoteright}s Hospital, Manchester University Hospitals NHS Foundation Trust Manchester Academic Health Sciences Centre, Manchester, United Kingdom; 45Center for Human Genetics Inc, Cambridge, MA, USA; 46Department of Pediatrics, Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan; 47Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, NH, USA; 48Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany; 49Gemeinschaftspraxis f{\"u}r Humangenetik Homburg/ Saar, Homburg, Germany; 50Department of Medical Genetics, Osaka Women{\textquoteright}s and Children{\textquoteright}s Hospital, Osaka, Japan; 51Willem Alexander Children{\textquoteright}s Hospital, Leiden University Medical Center, Leiden, The Netherlands; 52CRMR D{\'e}ficiences intellectuelles, Service de G{\'e}n{\'e}tique M{\'e}dicale, CLAD Ouest CHU H{\^o}pital Sud, Rennes, France; 53All Wales Medical Genetics Service, Glan Clwyd Hospital, Rhyl, United Kingdom; 54Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; 55Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada; 56The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, Toronto, ON, Canada; 57Department of Medical Genetics, CHU Bordeaux, Bordeaux, France; 58Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands; 59Genpute Computation Technologies Company, Istanbul, Turkey; 60Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands; 61Servicio de Pediatr{\'i}a, Hospital Universitario Doctor Peset, Valencia, Spain; 62Department of Pediatric Genetics, Ihsan Dogramaci Children{\textquoteright}s Hospital, Hacettepe University School of Medicine, Ankara, Turkey; 63Jacinto de Magalh{\~a}es Medical Genetics Center, Centro Hospitalar do Porto, Porto, Portugal; 64Departamento de neurometab{\'o}licas, Hospital Universitario Son Espases, Palma de Mallorca, Spain; 65Karadeniz Technical University, Faculty of Medicine, Dept of Child Neurology, Retired Professor, Trabzon, Turkey; 66Northern Genetics Service, Institute of Genetics Medicine, Newcastle upon Tyne, United Kingdom; 67Division of Pediatrics, Yamagata Prefectural and Sakata Munici pal Hospital Organization Nihon-Kai General Hospital, Sakata, Japan; 68Enva Engineering, Ankara, Turkey; 69Division of Neurology, Department of Pediatrics, Children{\textquoteright}s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada; 70Department of Genetics, H{\^o}pital Universitaire des Enfants Reine Fabiola, ULB Center of Medical Genetics, Universit{\'e} Libre de Bruxelles, Brussels, Belgium; 71Department of Genetics, H{\^o}pital Erasme. ULB Center of Medical Genetics, Universit{\'e} Libre de Bruxelles, Brussels, Belgium; 72Service de g{\'e}n{\'e}tique clinique Guy Fontaine, CHRU de Lille–H{\^o}pital Jeanne de Flandre, Lille, France; 73Division of Genetics, Arnold Palmer Hospital, Orlando, FL, USA; 74KinderGenome Genetics, Medical City Hospital Dallas, Dallas, TX, USA; 75Institute of Human Genetics, University Medical Center G{\"o}ttingen, G{\"o}ttingen, Germany; 76Center for Medical Genetics, Shinshu University Hospital, Matsumoto, Japan; 77Institute of Human Genetics, Medical Faculty, Heinrich-Heine-University, D{\"u}sseldorf, Germany; 78Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA Publisher Copyright: {\textcopyright} 2019, The Author(s). Copyright: Copyright 2019 Elsevier B.V., All rights reserved.",

year = "2019",

month = sep,

day = "1",

doi = "https://doi.org/10.1038/s41436-018-0368-y",

language = "English",

volume = "21",

pages = "2160--2161",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Lippincott Williams and Wilkins",

number = "9",

}

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, HL, 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, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)', Genetics in medicine, vol. 21, no. 9, pp. 2160-2161. https://doi.org/10.1038/s41436-018-0368-y

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z). / van der Sluijs, Pleuntje J.; Jansen, Sandra; Vergano, Samantha A. et al.
In: Genetics in medicine, Vol. 21, No. 9, 01.09.2019, p. 2160-2161.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

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, H. lya

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.

N1 - Funding Information: and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China; 19Center for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium; 20Center for Medical Genetics, Vrije Universiteit Brussels, Brussels, Belgium; 21Hunter Genetics and University of Newcastle, GrowUpWell Priority Research Centre, Newcastle, Australia; 22Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA; 23Department of Pediatric Genetics, Marmara University Pendik Hospital, Istanbul, Turkey; 24Department of Pediatrics and Genetics, University of Colorado Denver School of Medicine, Aurora, CO, USA; 25Department of Clinical Genetics, Odense University Hospital, Odense, Denmark; 26Department of Genetics, Cruces University Hospital, Biocruces Health Research Institute, Vizcayam, Spain; 27University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands; 28Department of Rehabilitation Medicine, Leiden University Medical Center, Leiden, The Netherlands; 29Institute for Medical Genetics and Human Genetics, Charité Universitätsmedizin, Berlin, Germany; 30Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom; 31Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan; 32Medical Genetics Department, Koç University School of Medicine (KUSoM), İstanbul, Turkey; 33Department of Clinical Genetics, Sophia Children’s Hospital, Erasmus MC, Rotterdam, The Netherlands; 34Department of Pediatric Genetics, Hematology Oncology Research & Training Children’s Hospital, Ankara, Turkey; 35Department of Medical Genetics, Dayton Children’s Hospital, Dayton, OH, USA; 36Department of Paediatrics, Odense University Hospital, Odense, Denmark; 37Department of Clinical Genetics, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom; 38Sección de Genética Médica, Servicio de Pediatria, Hospital Clinico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, CIBERERISCIII, Murcia, Spain; 39Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; 40Unidad de Genética, Hospital Universitario y Politécnico La Fe, Valencia, Spain; 41Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA; 42Northern Ireland Regional Genetics Centre, Belfast City Hospital, Belfast, Ireland; 43East Anglian Regional Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke’s Hospital, Cambridge, United Kingdom; 44Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, St Mary’s Hospital, Manchester University Hospitals NHS Foundation Trust Manchester Academic Health Sciences Centre, Manchester, United Kingdom; 45Center for Human Genetics Inc, Cambridge, MA, USA; 46Department of Pediatrics, Central Hospital, Aichi Human Service Center, Kasugai, Aichi, Japan; 47Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, NH, USA; 48Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany; 49Gemeinschaftspraxis für Humangenetik Homburg/ Saar, Homburg, Germany; 50Department of Medical Genetics, Osaka Women’s and Children’s Hospital, Osaka, Japan; 51Willem Alexander Children’s Hospital, Leiden University Medical Center, Leiden, The Netherlands; 52CRMR Déficiences intellectuelles, Service de Génétique Médicale, CLAD Ouest CHU Hôpital Sud, Rennes, France; 53All Wales Medical Genetics Service, Glan Clwyd Hospital, Rhyl, United Kingdom; 54Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; 55Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada; 56The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, Toronto, ON, Canada; 57Department of Medical Genetics, CHU Bordeaux, Bordeaux, France; 58Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands; 59Genpute Computation Technologies Company, Istanbul, Turkey; 60Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands; 61Servicio de Pediatría, Hospital Universitario Doctor Peset, Valencia, Spain; 62Department of Pediatric Genetics, Ihsan Dogramaci Children’s Hospital, Hacettepe University School of Medicine, Ankara, Turkey; 63Jacinto de Magalhães Medical Genetics Center, Centro Hospitalar do Porto, Porto, Portugal; 64Departamento de neurometabólicas, Hospital Universitario Son Espases, Palma de Mallorca, Spain; 65Karadeniz Technical University, Faculty of Medicine, Dept of Child Neurology, Retired Professor, Trabzon, Turkey; 66Northern Genetics Service, Institute of Genetics Medicine, Newcastle upon Tyne, United Kingdom; 67Division of Pediatrics, Yamagata Prefectural and Sakata Munici pal Hospital Organization Nihon-Kai General Hospital, Sakata, Japan; 68Enva Engineering, Ankara, Turkey; 69Division of Neurology, Department of Pediatrics, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada; 70Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, ULB Center of Medical Genetics, Université Libre de Bruxelles, Brussels, Belgium; 71Department of Genetics, Hôpital Erasme. ULB Center of Medical Genetics, Université Libre de Bruxelles, Brussels, Belgium; 72Service de génétique clinique Guy Fontaine, CHRU de Lille–Hôpital Jeanne de Flandre, Lille, France; 73Division of Genetics, Arnold Palmer Hospital, Orlando, FL, USA; 74KinderGenome Genetics, Medical City Hospital Dallas, Dallas, TX, USA; 75Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany; 76Center for Medical Genetics, Shinshu University Hospital, Matsumoto, Japan; 77Institute of Human Genetics, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany; 78Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA Publisher Copyright: © 2019, The Author(s). Copyright: Copyright 2019 Elsevier B.V., All rights reserved.

PY - 2019/9/1

Y1 - 2019/9/1

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.

UR - http://www.scopus.com/inward/record.url?scp=85060910177&partnerID=8YFLogxK

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060910177&origin=inward

UR - https://www.ncbi.nlm.nih.gov/pubmed/30696996

U2 - https://doi.org/10.1038/s41436-018-0368-y

DO - https://doi.org/10.1038/s41436-018-0368-y

M3 - Comment/Letter to the editor

C2 - 30696996

SN - 1098-3600

VL - 21

SP - 2160

EP - 2161

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 9

ER -

van der Sluijs PJ, Jansen S, Vergano SA, Adachi-Fukuda M, Alanay Y, AlKindy A et al. Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z). Genetics in medicine. 2019 Sept 1;21(9):2160-2161. Epub 2019 Jan 29. doi: https://doi.org/10.1038/s41436-018-0368-y

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

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