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Correction: The genomic and clinical landscape of fetal akinesia.
Pergande, Matthias; Motameny, Susanne; Özdemir, Özkan; Kreutzer, Mona; Wang, Haicui; Daimagüler, Hülya-Sevcan; Becker, Kerstin; Karakaya, Mert; Ehrhardt, Harald; Elcioglu, Nursel; Ostojic, Slavica; Chao, Cho-Ming; Kawalia, Amit; Duman, Özgür; Koy, Anne; Hahn, Andreas; Reimann, Jens; Schoner, Katharina; Schänzer, Anne; Westhoff, Jens H; Schwaibold, Eva Maria Christina; Cossee, Mireille; Imbert-Bouteille, Marion; von Pein, Harald; Haliloglu, Göknur; Topaloglu, Haluk; Altmüller, Janine; Nürnberg, Peter; Thiele, Holger; Heller, Raoul; Cirak, Sebahattin.
Afiliação
  • Pergande M; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Motameny S; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Özdemir Ö; University of Cologne, Cologne Center for Genomics CCG, Cologne, Germany.
  • Kreutzer M; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Wang H; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Daimagüler HS; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Becker K; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Karakaya M; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Ehrhardt H; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Elcioglu N; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Ostojic S; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Chao CM; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Kawalia A; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • Duman Ö; University of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Koy A; University of Cologne, University Hospital Cologne, Institute of Human Genetics, Cologne, Germany.
  • Hahn A; Department of General Pediatrics and Neonatology, Justus-Liebig-University, Gießen, Germany.
  • Reimann J; Department of Pediatric Genetics, Marmara University Medical School, Istanbul, Turkey.
  • Schoner K; Eastern Mediterranean University Medical School, Mersin, Turkey.
  • Schänzer A; Department of Neurology, Mother and Child Health Care Institute of Serbia "Dr. Vukan Cupic", Belgrade, Serbia.
  • Westhoff JH; Department of General Pediatrics and Neonatology, Justus-Liebig-University, Gießen, Germany.
  • Schwaibold EMC; University of Cologne, Cologne Center for Genomics CCG, Cologne, Germany.
  • Cossee M; Department of Pediatric Neurology, Akdeniz University Hospital, Antalya, Turkey.
  • Imbert-Bouteille M; University of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
  • von Pein H; Department of Pediatric Neurology, Social Pediatrics and Epileptology, Justus-Liebig-University, Gießen, Germany.
  • Haliloglu G; Department of Neurology, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Topaloglu H; Institute of Pathology, Philipps University of Marburg, Marburg, Germany.
  • Altmüller J; Institute of Neuropathology, Justus-Liebig-University, Gießen, Germany.
  • Nürnberg P; Heidelberg University, University Children's Hospital Heidelberg, Department of Pediatrics, Heidelberg, Germany.
  • Thiele H; Institute of Human Genetics, Heidelberg University, Institute of Human Genetics, Heidelberg, Germany.
  • Heller R; University of Montpellier, University Hospital of Montpellier, Molecular Diagnostic Laboratory, Montpellier, France.
  • Cirak S; University of Montpellier, University Hospital of Montpellier, Medical Genetics Department, Montpellier, France.
Genet Med ; 22(8): 1426-1428, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32451403
ABSTRACT
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 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article