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Imprinting disorders.
Eggermann, Thomas; Monk, David; de Nanclares, Guiomar Perez; Kagami, Masayo; Giabicani, Eloïse; Riccio, Andrea; Tümer, Zeynep; Kalish, Jennifer M; Tauber, Maithé; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R; Begemann, Matthias; Elbracht, Miriam.
Afiliación
  • Eggermann T; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany. teggermann@ukaachen.de.
  • Monk D; School of Biological Sciences, University of East Anglia, Norwich, UK.
  • de Nanclares GP; Rare Diseases Research Group, Molecular (Epi)Genetics Laboratory, Bioaraba Research Health Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, Spain.
  • Kagami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
  • Giabicani E; Sorbonne Université, INSERM, Centre de Recherche Saint-Antoine, APHP, Hôpital Armand Trousseau, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.
  • Riccio A; Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Università della Campania Luigi Vanvitelli, Caserta, Italy.
  • Tümer Z; Institute of Genetics and Biophysics A. Buzzati-Traverso, CNR, Naples, Italy.
  • Kalish JM; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Tauber M; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Duis J; Division of Human Genetics and Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the Departments of Pediatrics and Genetics at the Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Weksberg R; Centre de Référence Maladies Rares PRADORT (syndrome de PRADer-Willi et autres Obésités Rares avec Troubles du comportement alimentaire), Hôpital des Enfants, CHU Toulouse, Toulouse, France.
  • Maher ER; Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity) INSERM UMR1291 - CNRS UMR5051 - Université Toulouse III, Toulouse, France.
  • Begemann M; Department of Pediatrics, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Elbracht M; Division of Clinical and Metabolic Genetics, Department of Paediatrics and Genetics and Genome Biology Program, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.
Nat Rev Dis Primers ; 9(1): 33, 2023 Jun 29.
Article en En | MEDLINE | ID: mdl-37386011

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nat Rev Dis Primers Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nat Rev Dis Primers Año: 2023 Tipo del documento: Article País de afiliación: Alemania