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Surveillance of multiple congenital anomalies; searching for new associations.
Morris, Joan K; Bergman, Jorieke E H; Barisic, Ingeborg; Wellesley, Diana; Tucker, David; Limb, Elizabeth; Addor, Marie-Claude; Cavero-Carbonell, Clara; Matias Dias, Carlos; Draper, Elisabeth S; Echevarría-González-de-Garibay, Luis Javier; Gatt, Miriam; Klungsøyr, Kari; Lelong, Nathalie; Luyt, Karen; Materna-Kiryluk, Anna; Nelen, Vera; Neville, Amanda; Perthus, Isabelle; Pierini, Anna; Randrianaivo-Ranjatoelina, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Sayers, Geraldine; Wertelecki, Wladimir; Kinsner-Ovaskainen, Agnieszka; Garne, Ester.
Afiliación
  • Morris JK; Population Health Research Institute, St George's, University of London, London, UK. jmorris@sgul.ac.uk.
  • Bergman JEH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Wellesley D; Clinical Genetics, University of Southampton and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
  • Tucker D; Congenital Anomaly Register & Information Service for Wales (CARIS) Public Health Knowledge and Research, Public Health Wales, Swansea, Wales, UK.
  • Limb E; Population Health Research Institute, St George's, University of London, London, UK.
  • Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Matias Dias C; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.
  • Draper ES; Department of Population Health Sciences, Georg Davies Centre, University of Leicester, Leicester, UK.
  • Echevarría-González-de-Garibay LJ; Department of Health of the Basque Government, Vitoria-Gasteiz, Spain.
  • Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Guardamangia, Malta.
  • Klungsøyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Lelong N; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.
  • Luyt K; Université Paris Cité, CRESS, Équipe de recherche en épidémiologie obstétricale périnatale et pédiatrique (EPOPé), INSERM, INRA, Paris, France.
  • Materna-Kiryluk A; South West Congenital Anomaly Register, Bristol Medical School, University of Bristol, Bristol, UK.
  • Nelen V; Polish Registry of Congenital Malformations, Chair and Department of Medical Genetics, University of Medical Sciences, 61-701, Poznan, Poland.
  • Neville A; Provincial Institute for Hygiene, Antwerp, Belgium.
  • Perthus I; Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
  • Pierini A; Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
  • Randrianaivo-Ranjatoelina H; Unit of Epidemiology of Rare diseases and Congenital anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Rankin J; Service de Génétique Médicale et d'oncogénétique, Registre des Malformations Congénitales, Saint Pierre, La Réunion, France.
  • Rissmann A; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Rouget F; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University-Magdeburg, Magdeburg, Germany.
  • Sayers G; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000, Rennes, France.
  • Wertelecki W; Health Intelligence, Research and Development Health Service Executive, Dublin, Ireland.
  • Kinsner-Ovaskainen A; OMNI-Net Ukraine Programs, Rivne, Ukraine.
  • Garne E; European Commission, Joint Research Centre, Ispra, Italy.
Eur J Hum Genet ; 32(4): 407-412, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38052905
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Anomalías Congénitas / Anomalías Múltiples País/Región como asunto: Europa Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Anomalías Congénitas / Anomalías Múltiples País/Región como asunto: Europa Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article