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Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.
Martin-Almedina, Silvia; Ogmen, Kazim; Sackey, Ege; Grigoriadis, Dionysios; Karapouliou, Christina; Nadarajah, Noeline; Ebbing, Cathrine; Lord, Jenny; Mellis, Rhiannon; Kortuem, Fanny; Dinulos, Mary Beth; Polun, Cassandra; Bale, Sherri; Atton, Giles; Robinson, Alexandra; Reigstad, Hallvard; Houge, Gunnar; von der Wense, Axel; Becker, Wolf-Henning; Jeffery, Steve; Mortimer, Peter S; Gordon, Kristiana; Josephs, Katherine S; Robart, Sarah; Kilby, Mark D; Vallee, Stephanie; Gorski, Jerome L; Hempel, Maja; Berland, Siren; Mansour, Sahar; Ostergaard, Pia.
Afiliação
  • Martin-Almedina S; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Ogmen K; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Sackey E; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Grigoriadis D; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Karapouliou C; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Nadarajah N; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Ebbing C; Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.
  • Lord J; Wellcome Sanger Institute, Hinxton, UK.
  • Mellis R; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Kortuem F; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Dinulos MB; Institute of Human Genetics, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
  • Polun C; Departments of Pediatrics - Section of Genetics and Child Development, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
  • Bale S; Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
  • Atton G; Department of Child Health, University of Missouri School of Medicine, Columbia, MO, USA.
  • Robinson A; GeneDx, 207 Perry Parkway, Gaithersburg, MD, USA.
  • Reigstad H; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Houge G; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • von der Wense A; University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom.
  • Becker WH; Neonatal intensive care unit, Children's Department, Haukeland University Hospital, Bergen, Norway.
  • Jeffery S; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
  • Mortimer PS; Department of Neonatology and Paediatric Intensive Care, Altona Children's Hospital, Hamburg, Germany.
  • Gordon K; Elbe Center for Prenatal Medicine, Hamburg, Germany.
  • Josephs KS; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Robart S; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Kilby MD; Dermatology & Lymphovascular Medicine, St George's Universities NHS Foundation Trust, London, UK.
  • Vallee S; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Gorski JL; Dermatology & Lymphovascular Medicine, St George's Universities NHS Foundation Trust, London, UK.
  • Hempel M; Molecular and Clinical Sciences Institute, St George's University of London, London, UK.
  • Berland S; South West Thames Regional Genetics Service, St George's NHS Foundation Trust, London, UK.
  • Mansour S; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Ostergaard P; The Institute of Metabolism & Systems Research, College of Medical & Dental Sciences, University of Birmingham, Birmingham, UK.
Genet Med ; 23(7): 1376-1377, 2021 Jul.
Article em En | MEDLINE | ID: mdl-34040196
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article