Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019
In the original version of this Article the author Solveig Heide was incorrectly given as Heide Solveig. There was also an error in the spelling of the author Sandra Whalen, which was given as Sandra Wallen. In addition, the affiliation for Sandra Whalen was mistakenly quoted as AP-HP, Département de Génétique, Centre de Référence Maladies Rares “Anomalies du développement et syndromes malformatifs” Hôpital de la Pitié Salpêtrière, Paris, France instead of UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France. All errors are now corrected in both the PDF and HTML versions of the Article.
Author information
These authors contributed equally: Paul A. Wade, Katherine Lachlan.
Authors and Affiliations
The Genetics Institute, Rambam Health Care Campus, Haifa, Israel
Karin Weiss MD, Alina Kurolap MSc, Tamar Paperna PhD & Hagit Baris Feldman MD
Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA
Hayley P. Lazar BSc, Motoki Takaku PhD, John D. Roberts PhD, Robert M. Petrovich PhD & Paul A. Wade PhD
The Ruth and Bruce Rappaport Faculty of Medicine, Technion–Israel Institute of Technology, Haifa, Israel
Alina Kurolap MSc & Hagit Baris Feldman MD
Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
Ariel F. Martinez PhD, Mahim Jain MD PhD & Maximilian Muenke MD
Genetics Institute, Schneider Children’s Medical Center, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Lior Cohen MD
Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway
Marie F. Smeland MD
UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France
Sandra Whalen MD
AP-HP, Département de Génétique, Centre de Référence Maladies Rares “Anomalies du développement et syndromes malformatifs” Hôpital de la Pitié Salpêtrière, Paris, France
Solveig Heide MD & Boris Keren MD PhD
Department of Genetics, Utrecht University Medical Center, Utrecht, the Netherlands
Pauline Terhal MD
Department of Clinical Genetics, Guy’s Hospital, London, UK
Melita Irving MD
Division of Medical Genetics and Metabolism, Children’s Hospital of The King’s Daughters, Norfolk, VA, USA
Samantha A. Schrier Vergano MD & Amy Kenney MSc
Department of Pediatrics, Eastern Virginia Medical School, Norfolk, VA, USA
Samantha A. Schrier Vergano MD
Centre for Rare Diseases, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Hanne Hove MD
Division of Genomic Diagnostics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Elizabeth DeChene MSc, Avni Santani PhD & Bryan Krock PhD
Department of Pediatrics, Division of Genetics, Metabolism and Genomic Medicine, University of Michigan, Ann Arbor, MI, USA
Shane C. Quinonez MD
Department of Biochemistry and Genetics, University Hospital Angers, Angers, France
Estelle Colin MD & Alban Ziegler MD
Banner Child Neurology, Glendale, AZ, USA
Melissa Rumple MSc
Bone and Osteogenesis Imperfecta Department, Kennedy Krieger Institute, Baltimore, MD, USA
Mahim Jain MD PhD
Department of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA, USA
Danielle Monteil MD
Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA
Elizabeth R. Roeder MD & Kimberly Nugent MSc
Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
Arie van Haeringen MD
Department of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA
Michael Gambello MD PhD
Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Līvija Medne MSc, Cara M. Skraban MD & Elaine H. Zackai MD
Division of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Holly A. Dubbs MSc
Department of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France
Thomas Smol MD & Jamal Ghoumid MD
EA7364 RADEME (Research Team on Rare Developmental and Metabolic Diseases), Lille 2 University, Lille, France
Thomas Smol MD & Jamal Ghoumid MD
Sheffield Children’s Hospital NHS Foundation Trust, Western Bank, Sheffield, UK
Michael J. Parker MD
Northern Genetics Service, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK
Michael Wright MD
University of Exeter Medical School, Clinical Genetics Royal Devon & Exeter Hospital, Exeter, UK
Peter Turnpenny MD
Institute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
Jill Clayton-Smith MD & Kay Metcalfe MD
Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK
Jill Clayton-Smith MD & Kay Metcalfe MD
Laboratory of Structural Biology, Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan
Hitoshi Kurumizaka PhD
Mindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Bruce D. Gelb MD
Department of Pediatrics, University of Montreal and CHU Sainte-Justine, Montreal, QC, Canada
Philippe M. Campeau MD
Wessex Clinical Genetics Service, University Hospital Southampton NHS Trust. Department of Human Genetics and Genomic Medicine, Southampton University, Southampton, UK
Katherine Lachlan MD
- Karin Weiss MD
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Corresponding author
Correspondence to Karin Weiss MD.
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Weiss, K., Lazar, H.P., Kurolap, A. et al. Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis. Genet Med 22, 669 (2020). https://doi.org/10.1038/s41436-019-0727-3
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DOI: https://doi.org/10.1038/s41436-019-0727-3
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