Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2019-03-01
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| Series: | Genome Medicine |
| Online Access: | http://link.springer.com/article/10.1186/s13073-019-0630-1 |
| _version_ | 1811325485829849088 |
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| author | Francesco Vetrini Shane McKee Jill A. Rosenfeld Mohnish Suri Andrea M. Lewis Kimberly Margaret Nugent Elizabeth Roeder Rebecca O. Littlejohn Sue Holder Wenmiao Zhu Joseph T. Alaimo Brett Graham Jill M. Harris James B. Gibson Matthew Pastore Kim L. McBride Makanko Komara Lihadh Al-Gazali Aisha Al Shamsi Elizabeth A. Fanning Klaas J. Wierenga Daryl A. Scott Ziva Ben-Neriah Vardiella Meiner Hanoch Cassuto Orly Elpeleg J. Lloyd Holder Jr Lindsay C. Burrage Laurie H. Seaver Lionel Van Maldergem Sonal Mahida Janet S. Soul Margaret Marlatt Ludmila Matyakhina Julie Vogt June-Anne Gold Soo-Mi Park Vinod Varghese Anne K. Lampe Ajith Kumar Melissa Lees Muriel Holder-Espinasse Vivienne McConnell Birgitta Bernhard Ed Blair Victoria Harrison The DDD study Donna M. Muzny Richard A. Gibbs Sarah H. Elsea Jennifer E. Posey Weimin Bi Seema Lalani Fan Xia Yaping Yang Christine M. Eng James R. Lupski Pengfei Liu |
| author_facet | Francesco Vetrini Shane McKee Jill A. Rosenfeld Mohnish Suri Andrea M. Lewis Kimberly Margaret Nugent Elizabeth Roeder Rebecca O. Littlejohn Sue Holder Wenmiao Zhu Joseph T. Alaimo Brett Graham Jill M. Harris James B. Gibson Matthew Pastore Kim L. McBride Makanko Komara Lihadh Al-Gazali Aisha Al Shamsi Elizabeth A. Fanning Klaas J. Wierenga Daryl A. Scott Ziva Ben-Neriah Vardiella Meiner Hanoch Cassuto Orly Elpeleg J. Lloyd Holder Jr Lindsay C. Burrage Laurie H. Seaver Lionel Van Maldergem Sonal Mahida Janet S. Soul Margaret Marlatt Ludmila Matyakhina Julie Vogt June-Anne Gold Soo-Mi Park Vinod Varghese Anne K. Lampe Ajith Kumar Melissa Lees Muriel Holder-Espinasse Vivienne McConnell Birgitta Bernhard Ed Blair Victoria Harrison The DDD study Donna M. Muzny Richard A. Gibbs Sarah H. Elsea Jennifer E. Posey Weimin Bi Seema Lalani Fan Xia Yaping Yang Christine M. Eng James R. Lupski Pengfei Liu |
| author_sort | Francesco Vetrini |
| collection | DOAJ |
| description | It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated. |
| first_indexed | 2024-04-13T14:34:00Z |
| format | Article |
| id | doaj.art-9deb62b3cdbb447d9597c9b55e926986 |
| institution | Directory Open Access Journal |
| issn | 1756-994X |
| language | English |
| last_indexed | 2024-04-13T14:34:00Z |
| publishDate | 2019-03-01 |
| publisher | BMC |
| record_format | Article |
| series | Genome Medicine |
| spelling | doaj.art-9deb62b3cdbb447d9597c9b55e9269862022-12-22T02:43:05ZengBMCGenome Medicine1756-994X2019-03-011111210.1186/s13073-019-0630-1Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndromeFrancesco Vetrini0Shane McKee1Jill A. Rosenfeld2Mohnish Suri3Andrea M. Lewis4Kimberly Margaret Nugent5Elizabeth Roeder6Rebecca O. Littlejohn7Sue Holder8Wenmiao Zhu9Joseph T. Alaimo10Brett Graham11Jill M. Harris12James B. Gibson13Matthew Pastore14Kim L. McBride15Makanko Komara16Lihadh Al-Gazali17Aisha Al Shamsi18Elizabeth A. Fanning19Klaas J. Wierenga20Daryl A. Scott21Ziva Ben-Neriah22Vardiella Meiner23Hanoch Cassuto24Orly Elpeleg25J. Lloyd Holder Jr26Lindsay C. Burrage27Laurie H. Seaver28Lionel Van Maldergem29Sonal Mahida30Janet S. Soul31Margaret Marlatt32Ludmila Matyakhina33Julie Vogt34June-Anne Gold35Soo-Mi Park36Vinod Varghese37Anne K. Lampe38Ajith Kumar39Melissa Lees40Muriel Holder-Espinasse41Vivienne McConnell42Birgitta Bernhard43Ed Blair44Victoria Harrison45The DDD study46Donna M. Muzny47Richard A. Gibbs48Sarah H. Elsea49Jennifer E. Posey50Weimin Bi51Seema Lalani52Fan Xia53Yaping Yang54Christine M. Eng55James R. Lupski56Pengfei Liu57Baylor GeneticsNorthern Ireland Regional Genetics Service, Belfast City HospitalDepartment of Molecular and Human Genetics, Baylor College of MedicineNottingham Genetics Service, Nottingham City HospitalDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Molecular and Human Genetics, Baylor College of MedicineNorth West Thames Regional Genetics Service, 759 Northwick Park HospitalBaylor GeneticsDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Molecular and Human Genetics, Baylor College of MedicineDell Children’s Medical GroupDell Children’s Medical GroupDivision of Genetic and Genomic Medicine, Nationwide Children’s Hospital; and Department of Pediatrics, College of Medicine, Ohio State UniversityDivision of Genetic and Genomic Medicine, Nationwide Children’s Hospital; and Department of Pediatrics, College of Medicine, Ohio State UniversityDepartment of Pediatrics, College of Medicine & Health Sciences, United Arab UniversityDepartment of Pediatrics, College of Medicine & Health Sciences, United Arab UniversityDepartment of Pediatrics, Tawam HospitalDepartment of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences CenterDepartment of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences CenterDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical CenterDepartment of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical CenterThe Hebrew University of JerusalemMonique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical CenterDepartment of Pediatrics, Texas Children’s HospitalDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Pediatrics, University of HawaiiCentre de Génétique Humaine, Université de Franche-ComtéDepartment of Neurology, Boston Children’s HospitalDepartment of Neurology, Boston Children’s HospitalDepartment of Neurology, Boston Children’s HospitalGene DXWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Women’s and Children’s Hospitals NHS Foundation TrustEast Anglia Regional Genetics Service, Addenbrooke’s HospitalEast Anglia Regional Genetics Service, Addenbrooke’s HospitalAll-Wales Medical Genetics Service, University Hospital of WalesSouth East of Scotland Clinical Genetic Service, Western General HospitalNorth East Thames Regional Genetics Service, Great Ormond Street HospitalNorth East Thames Regional Genetics Service, Great Ormond Street HospitalSouth East Thames Regional Genetics Service, Guy’s HospitalNorthern Ireland Regional Genetics Service, Belfast City HospitalNorth West Thames Regional Genetics Service, 759 Northwick Park HospitalOxford Regional Genetics Service, Oxford University HospitalsWessex Clinical Genetics Service, Princess Anne HospitalThe DDD Study, Wellcome Trust Sanger InstituteDepartment of Molecular and Human Genetics, Baylor College of MedicineDepartment of Molecular and Human Genetics, Baylor College of MedicineBaylor GeneticsDepartment of Molecular and Human Genetics, Baylor College of MedicineBaylor GeneticsBaylor GeneticsBaylor GeneticsBaylor GeneticsBaylor GeneticsBaylor GeneticsBaylor GeneticsIt was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.http://link.springer.com/article/10.1186/s13073-019-0630-1 |
| spellingShingle | Francesco Vetrini Shane McKee Jill A. Rosenfeld Mohnish Suri Andrea M. Lewis Kimberly Margaret Nugent Elizabeth Roeder Rebecca O. Littlejohn Sue Holder Wenmiao Zhu Joseph T. Alaimo Brett Graham Jill M. Harris James B. Gibson Matthew Pastore Kim L. McBride Makanko Komara Lihadh Al-Gazali Aisha Al Shamsi Elizabeth A. Fanning Klaas J. Wierenga Daryl A. Scott Ziva Ben-Neriah Vardiella Meiner Hanoch Cassuto Orly Elpeleg J. Lloyd Holder Jr Lindsay C. Burrage Laurie H. Seaver Lionel Van Maldergem Sonal Mahida Janet S. Soul Margaret Marlatt Ludmila Matyakhina Julie Vogt June-Anne Gold Soo-Mi Park Vinod Varghese Anne K. Lampe Ajith Kumar Melissa Lees Muriel Holder-Espinasse Vivienne McConnell Birgitta Bernhard Ed Blair Victoria Harrison The DDD study Donna M. Muzny Richard A. Gibbs Sarah H. Elsea Jennifer E. Posey Weimin Bi Seema Lalani Fan Xia Yaping Yang Christine M. Eng James R. Lupski Pengfei Liu Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome Genome Medicine |
| title | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_full | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_fullStr | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_full_unstemmed | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_short | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_sort | correction to de novo and inherited tcf20 pathogenic variants are associated with intellectual disability dysmorphic features hypotonia and neurological impairments with similarities to smith magenis syndrome |
| url | http://link.springer.com/article/10.1186/s13073-019-0630-1 |
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