Your browser doesn't support javascript.
loading
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply.
Brioude, Frédéric; Hennekam, Raoul; Bliek, Jet; Coze, Carole; Eggermann, Thomas; Ferrero, Giovanni B; Kratz, Christian; Bouc, Yves Le; Maas, Saskia M; Mackay, Deborah J G; Maher, Eamonn R; Mussa, Alessandro; Netchine, Irene.
Afiliação
  • Brioude F; Sorbonne Université, INSERM UMR_S938 Centre de Recherche Saint-Antoine, AP-HP, Hôpital Trousseau, F-75012, Paris, France. frederic.brioude@aphp.fr.
  • Hennekam R; Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Bliek J; Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Coze C; Aix-Marseille Univ, Assistance Publique Hôpitaux de Marseille (APHM), Hôpital d'Enfants de La Timone, Service d'Hématologie-Oncologie Pédiatrique, Marseille, France.
  • Eggermann T; Institute of Human Genetics, University Hospital, Technical University of Aachen, Aachen, Germany.
  • Ferrero GB; Department of Public Health and Pediatric Sciences, University of Torino, Torino, Italy.
  • Kratz C; Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
  • Bouc YL; Sorbonne Université, INSERM UMR_S938 Centre de Recherche Saint-Antoine, AP-HP, Hôpital Trousseau, F-75012, Paris, France.
  • Maas SM; Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Mackay DJG; Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Maher ER; Department of Medical Genetics, University of Cambridge and NIHR Cambridge Biomedical Research Centre and Cancer Research UK Cambridge Centre, Cambridge Biomedical Campus, Cambridge, UK.
  • Mussa A; Department of Public Health and Pediatric Sciences, University of Torino, Torino, Italy.
  • Netchine I; Neonatal Intensive Care Unit, Department of Gynaecology and Obstetrics, S.Anna Hospital, Città della Salute e della Scienza di Torino, Torino, Italy.
Eur J Hum Genet ; 26(4): 471-472, 2018 04.
Article em En | MEDLINE | ID: mdl-29449718
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Tumor de Wilms Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Tumor de Wilms Idioma: En Ano de publicação: 2018 Tipo de documento: Article