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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

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Title: Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Authors: Blok LS; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Rousseau J; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada., Twist J; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA., Ehresmann S; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada., Takaku M; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA., Venselaar H; Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Rodan LH; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA., Nowak CB; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA., Douglas J; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA., Swoboda KJ; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA., Steeves MA; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA., Sahai I; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA., Stumpel CTRM; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Stegmann APA; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Wheeler P; Nemours Childrens Clinic, Orlando, FL, 32827, USA., Willing M; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA., Fiala E; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA., Kochhar A; Valley Children's Hospital, Madera, CA, 93636, USA., Gibson WT; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada., Cohen ASA; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada., Agbahovbe R; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada., Innes AM; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada., Au PYB; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada., Rankin J; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK., Anderson IJ; Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA., Skinner SA; Greenwood Genetic Center, Greenwood, SC, 29646, USA., Louie RJ; Greenwood Genetic Center, Greenwood, SC, 29646, USA., Warren HE; Greenwood Genetic Center, Greenwood, SC, 29646, USA., Afenjar A; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France., Keren B; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France., Nava C; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.; INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France., Buratti J; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France., Isapof A; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases 'Nord/Est/Ile-de-France', FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France., Rodriguez D; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France., Lewandowski R; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA., Propst J; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA., van Essen T; Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands., Choi M; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea., Lee S; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea., Chae JH; Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea., Price S; Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK., Schnur RE; GeneDx, Gaithersburg, MD, 20877, USA., Douglas G; GeneDx, Gaithersburg, MD, 20877, USA., Wentzensen IM; GeneDx, Gaithersburg, MD, 20877, USA., Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany., Reis A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany., Bialer MG; Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA., Moore C; Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA., Koopmans M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Brilstra EH; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Monroe GR; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., van Gassen KLI; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Newbury-Ecob R; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK., Bownass L; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK., Bader I; Department of Clinical Genetics, University Children's Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria., Mayr JA; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria., Wortmann SB; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.; Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany., Jakielski KJ; Communication Sciences and Disorders, Augustana College, Rock Island, IL, 61201, USA., Strand EA; Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA., Kloth K; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany., Bierhals T; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany., Roberts JD; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA., Petrovich RM; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA., Machida S; Waseda University, Tokyo, 169-8050, Japan., Kurumizaka H; Waseda University, Tokyo, 169-8050, Japan., Lelieveld S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Jansen S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Deriziotis P; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands., Faivre L; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Thevenon J; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Assoum M; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Shriberg L; Waisman Center, Phonology Project, Madison, WI, 53705-2280, USA., Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Brunner HG; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Wade PA; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA., Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands. simon.fisher@mpi.nl.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands. simon.fisher@mpi.nl., Campeau PM; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada. p.campeau@umontreal.ca.; Sainte-Justine Hospital, University of Montreal, Montreal, QC, H3T 1C5, Canada. p.campeau@umontreal.ca.
Corporate Authors: DDD study
Source: Nature communications [Nat Commun] 2019 Feb 15; Vol. 10 (1), pp. 883. Date of Electronic Publication: 2019 Feb 15.
Publication Type: Journal Article; Published Erratum
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
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  Data: <searchLink fieldCode="AU" term="%22Blok+LS%22">Blok LS</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Rousseau+J%22">Rousseau J</searchLink>; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.<br /><searchLink fieldCode="AU" term="%22Twist+J%22">Twist J</searchLink>; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.<br /><searchLink fieldCode="AU" term="%22Ehresmann+S%22">Ehresmann S</searchLink>; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.<br /><searchLink fieldCode="AU" term="%22Takaku+M%22">Takaku M</searchLink>; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.<br /><searchLink fieldCode="AU" term="%22Venselaar+H%22">Venselaar H</searchLink>; Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Rodan+LH%22">Rodan LH</searchLink>; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.<br /><searchLink fieldCode="AU" term="%22Nowak+CB%22">Nowak CB</searchLink>; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.<br /><searchLink fieldCode="AU" term="%22Douglas+J%22">Douglas J</searchLink>; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.<br /><searchLink fieldCode="AU" term="%22Swoboda+KJ%22">Swoboda KJ</searchLink>; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.<br /><searchLink fieldCode="AU" term="%22Steeves+MA%22">Steeves MA</searchLink>; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.<br /><searchLink fieldCode="AU" term="%22Sahai+I%22">Sahai I</searchLink>; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.<br /><searchLink fieldCode="AU" term="%22Stumpel+CTRM%22">Stumpel CTRM</searchLink>; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Stegmann+APA%22">Stegmann APA</searchLink>; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Wheeler+P%22">Wheeler P</searchLink>; Nemours Childrens Clinic, Orlando, FL, 32827, USA.<br /><searchLink fieldCode="AU" term="%22Willing+M%22">Willing M</searchLink>; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.<br /><searchLink fieldCode="AU" term="%22Fiala+E%22">Fiala E</searchLink>; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.<br /><searchLink fieldCode="AU" term="%22Kochhar+A%22">Kochhar A</searchLink>; Valley Children's Hospital, Madera, CA, 93636, USA.<br /><searchLink fieldCode="AU" term="%22Gibson+WT%22">Gibson WT</searchLink>; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.<br /><searchLink fieldCode="AU" term="%22Cohen+ASA%22">Cohen ASA</searchLink>; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.<br /><searchLink fieldCode="AU" term="%22Agbahovbe+R%22">Agbahovbe R</searchLink>; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.<br /><searchLink fieldCode="AU" term="%22Innes+AM%22">Innes AM</searchLink>; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.<br /><searchLink fieldCode="AU" term="%22Au+PYB%22">Au PYB</searchLink>; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.<br /><searchLink fieldCode="AU" term="%22Rankin+J%22">Rankin J</searchLink>; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK.<br /><searchLink fieldCode="AU" term="%22Anderson+IJ%22">Anderson IJ</searchLink>; Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA.<br /><searchLink fieldCode="AU" term="%22Skinner+SA%22">Skinner SA</searchLink>; Greenwood Genetic Center, Greenwood, SC, 29646, USA.<br /><searchLink fieldCode="AU" term="%22Louie+RJ%22">Louie RJ</searchLink>; Greenwood Genetic Center, Greenwood, SC, 29646, USA.<br /><searchLink fieldCode="AU" term="%22Warren+HE%22">Warren HE</searchLink>; Greenwood Genetic Center, Greenwood, SC, 29646, USA.<br /><searchLink fieldCode="AU" term="%22Afenjar+A%22">Afenjar A</searchLink>; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France.<br /><searchLink fieldCode="AU" term="%22Keren+B%22">Keren B</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.<br /><searchLink fieldCode="AU" term="%22Nava+C%22">Nava C</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.; INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France.<br /><searchLink fieldCode="AU" term="%22Buratti+J%22">Buratti J</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.<br /><searchLink fieldCode="AU" term="%22Isapof+A%22">Isapof A</searchLink>; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases 'Nord/Est/Ile-de-France', FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France.<br /><searchLink fieldCode="AU" term="%22Rodriguez+D%22">Rodriguez D</searchLink>; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France.<br /><searchLink fieldCode="AU" term="%22Lewandowski+R%22">Lewandowski R</searchLink>; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.<br /><searchLink fieldCode="AU" term="%22Propst+J%22">Propst J</searchLink>; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.<br /><searchLink fieldCode="AU" term="%22van+Essen+T%22">van Essen T</searchLink>; Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Choi+M%22">Choi M</searchLink>; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Lee+S%22">Lee S</searchLink>; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Chae+JH%22">Chae JH</searchLink>; Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Price+S%22">Price S</searchLink>; Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK.<br /><searchLink fieldCode="AU" term="%22Schnur+RE%22">Schnur RE</searchLink>; GeneDx, Gaithersburg, MD, 20877, USA.<br /><searchLink fieldCode="AU" term="%22Douglas+G%22">Douglas G</searchLink>; GeneDx, Gaithersburg, MD, 20877, USA.<br /><searchLink fieldCode="AU" term="%22Wentzensen+IM%22">Wentzensen IM</searchLink>; GeneDx, Gaithersburg, MD, 20877, USA.<br /><searchLink fieldCode="AU" term="%22Zweier+C%22">Zweier C</searchLink>; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany.<br /><searchLink fieldCode="AU" term="%22Reis+A%22">Reis A</searchLink>; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany.<br /><searchLink fieldCode="AU" term="%22Bialer+MG%22">Bialer MG</searchLink>; Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA.<br /><searchLink fieldCode="AU" term="%22Moore+C%22">Moore C</searchLink>; Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA.<br /><searchLink fieldCode="AU" term="%22Koopmans+M%22">Koopmans M</searchLink>; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Brilstra+EH%22">Brilstra EH</searchLink>; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Monroe+GR%22">Monroe GR</searchLink>; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Gassen+KLI%22">van Gassen KLI</searchLink>; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Binsbergen+E%22">van Binsbergen E</searchLink>; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Newbury-Ecob+R%22">Newbury-Ecob R</searchLink>; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK.<br /><searchLink fieldCode="AU" term="%22Bownass+L%22">Bownass L</searchLink>; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK.<br /><searchLink fieldCode="AU" term="%22Bader+I%22">Bader I</searchLink>; Department of Clinical Genetics, University Children's Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria.<br /><searchLink fieldCode="AU" term="%22Mayr+JA%22">Mayr JA</searchLink>; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.<br /><searchLink fieldCode="AU" term="%22Wortmann+SB%22">Wortmann SB</searchLink>; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.; Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany.<br /><searchLink fieldCode="AU" term="%22Jakielski+KJ%22">Jakielski KJ</searchLink>; Communication Sciences and Disorders, Augustana College, Rock Island, IL, 61201, USA.<br /><searchLink fieldCode="AU" term="%22Strand+EA%22">Strand EA</searchLink>; Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.<br /><searchLink fieldCode="AU" term="%22Kloth+K%22">Kloth K</searchLink>; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.<br /><searchLink fieldCode="AU" term="%22Bierhals+T%22">Bierhals T</searchLink>; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.<br /><searchLink fieldCode="AU" term="%22Roberts+JD%22">Roberts JD</searchLink>; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.<br /><searchLink fieldCode="AU" term="%22Petrovich+RM%22">Petrovich RM</searchLink>; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.<br /><searchLink fieldCode="AU" term="%22Machida+S%22">Machida S</searchLink>; Waseda University, Tokyo, 169-8050, Japan.<br /><searchLink fieldCode="AU" term="%22Kurumizaka+H%22">Kurumizaka H</searchLink>; Waseda University, Tokyo, 169-8050, Japan.<br /><searchLink fieldCode="AU" term="%22Lelieveld+S%22">Lelieveld S</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Pfundt+R%22">Pfundt R</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Jansen+S%22">Jansen S</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Deriziotis+P%22">Deriziotis P</searchLink>; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Faivre+L%22">Faivre L</searchLink>; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France.<br /><searchLink fieldCode="AU" term="%22Thevenon+J%22">Thevenon J</searchLink>; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France.<br /><searchLink fieldCode="AU" term="%22Assoum+M%22">Assoum M</searchLink>; Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France.<br /><searchLink fieldCode="AU" term="%22Shriberg+L%22">Shriberg L</searchLink>; Waisman Center, Phonology Project, Madison, WI, 53705-2280, USA.<br /><searchLink fieldCode="AU" term="%22Kleefstra+T%22">Kleefstra T</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Brunner+HG%22">Brunner HG</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Wade+PA%22">Wade PA</searchLink>; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.<br /><searchLink fieldCode="AU" term="%22Fisher+SE%22">Fisher SE</searchLink>; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands. simon.fisher@mpi.nl.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands. simon.fisher@mpi.nl.<br /><searchLink fieldCode="AU" term="%22Campeau+PM%22">Campeau PM</searchLink>; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada. p.campeau@umontreal.ca.; Sainte-Justine Hospital, University of Montreal, Montreal, QC, H3T 1C5, Canada. p.campeau@umontreal.ca.
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  Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2019 Feb 15; Vol. 10 (1), pp. 883. <i>Date of Electronic Publication: </i>2019 Feb 15.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Pub%2E+Group%22">Nature Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101528555 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2041-1723 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220411723%22">20411723 </searchLink><i>NLM ISO Abbreviation: </i>Nat Commun <i>Subsets: </i>PubMed not MEDLINE
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