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Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Weiss, Karin; Lazar, Hayley P; Kurolap, Alina; Martinez, Ariel F; Paperna, Tamar; Cohen, Lior; Smeland, Marie F; Whalen, Sandra; Heide, Solveig; Keren, Boris; Terhal, Pauline; Irving, Melita; Takaku, Motoki; Roberts, John D; Petrovich, Robert M; Vergano, Samantha A Schrier; Kenney, Amy; Hove, Hanne; DeChene, Elizabeth; Quinonez, Shane C; Colin, Estelle; Ziegler, Alban; Rumple, Melissa; Jain, Mahim; Monteil, Danielle; Roeder, Elizabeth R; Nugent, Kimberly; van Haeringen, Arie; Gambello, Michael; Santani, Avni; Medne, Livija; Krock, Bryan; Skraban, Cara M; Zackai, Elaine H; Dubbs, Holly A; Smol, Thomas; Ghoumid, Jamal; Parker, Michael J; Wright, Michael; Turnpenny, Peter; Clayton-Smith, Jill; Metcalfe, Kay; Kurumizaka, Hitoshi; Gelb, Bruce D; Feldman, Hagit Baris; Campeau, Philippe M; Muenke, Maximilian; Wade, Paul A; Lachlan, Katherine.
Afiliación
  • Weiss K; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel. k_weiss@rambam.health.gov.il.
  • Lazar HP; Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
  • Kurolap A; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
  • Martinez AF; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
  • Paperna T; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Cohen L; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
  • Smeland MF; Genetics Institute, Schneider Children's Medical Center, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Whalen S; Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
  • Heide S; UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France.
  • Keren B; AP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
  • Terhal P; AP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
  • Irving M; Department of Genetics, Utrecht University Medical Center, Utrecht, the Netherlands.
  • Takaku M; Department of Clinical Genetics, Guy's Hospital, London, UK.
  • Roberts JD; Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
  • Petrovich RM; Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
  • Vergano SAS; Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
  • Kenney A; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
  • Hove H; Department of Pediatrics, Eastern Virginia Medical School, Norfolk, VA, USA.
  • DeChene E; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
  • Quinonez SC; Centre for Rare Diseases, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Colin E; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Ziegler A; Department of Pediatrics, Division of Genetics, Metabolism and Genomic Medicine, University of Michigan, Ann Arbor, MI, USA.
  • Rumple M; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
  • Jain M; Department of Biochemistry and Genetics, University Hospital Angers, Angers, France.
  • Monteil D; Banner Child Neurology, Glendale, AZ, USA.
  • Roeder ER; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Nugent K; Bone and Osteogenesis Imperfecta Department, Kennedy Krieger Institute, Baltimore, MD, USA.
  • van Haeringen A; Department of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA, USA.
  • Gambello M; Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
  • Santani A; Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
  • Medne L; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Krock B; Department of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA.
  • Skraban CM; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Dubbs HA; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Smol T; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Ghoumid J; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Parker MJ; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Wright M; Department of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
  • Turnpenny P; EA7364 RADEME (Research Team on Rare Developmental and Metabolic Diseases), Lille 2 University, Lille, France.
  • Clayton-Smith J; Department of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
  • Metcalfe K; EA7364 RADEME (Research Team on Rare Developmental and Metabolic Diseases), Lille 2 University, Lille, France.
  • Kurumizaka H; Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield, UK.
  • Gelb BD; Northern Genetics Service, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK.
  • Feldman HB; University of Exeter Medical School, Clinical Genetics Royal Devon & Exeter Hospital, Exeter, UK.
  • Campeau PM; Institute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
  • Muenke M; Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK.
  • Wade PA; Institute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
  • Lachlan K; Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK.
Genet Med ; 22(3): 669, 2020 Mar.
Article en En | MEDLINE | ID: mdl-31844176
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Israel Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Israel Pais de publicación: Estados Unidos