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Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study.
Glinianaia, Svetlana V; Rankin, Judith; Tan, Joachim; Loane, Maria; Garne, Ester; Cavero-Carbonell, Clara; de Walle, Hermien E K; Gatt, Miriam; Gissler, Mika; Klungsøyr, Kari; Lelong, Natalie; Neville, Amanda; Pierini, Anna; Tucker, David F; Urhoj, Stine Kjaer; Wellesley, Diana Gay; Morris, Joan K.
Afiliación
  • Glinianaia SV; Newcastle University Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK svetlana.glinianaia@ncl.ac.uk.
  • Rankin J; Newcastle University Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Tan J; Population Health Research Institute, St George's University of London, London, UK.
  • Loane M; Centre for Maternal, Fetal and Infant Research, Faculty of Life and Health Sciences, Ulster University, Belfast, UK.
  • Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital - University Hospital of Southern Denmark, Kolding, Denmark.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, FISABIO, Valencia, Spain.
  • de Walle HEK; University Medical Centre Groningen, Department of Genetics, University of Groningen, Groningen, Netherlands.
  • Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Tal-Pietà, Malta.
  • Gissler M; Department of Knowledge Brokers, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Klungsøyr K; Academic Primary Health Care Centre, Stockholm, Region Stockholm, Sweden.
  • Lelong N; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Neville A; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.
  • Pierini A; Université de Paris Cité, Obstetrical, Perinatal and Paediatric Epidemiology Research Team (EPOPé), CRESS, INSERM, Paris, France.
  • Tucker DF; IMER Registry (Emilia Romagna Registry of Birth Defects), Centre for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Emilia-Romagna, Italy.
  • Urhoj SK; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Toscana, Italy.
  • Wellesley DG; Public Health Wales, Public Health Knowledge and Research, Swansea, Wales, UK.
  • Morris JK; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital - University Hospital of Southern Denmark, Kolding, Denmark.
Arch Dis Child ; 108(6): 461-467, 2023 06.
Article en En | MEDLINE | ID: mdl-36882305
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Arch Dis Child Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Arch Dis Child Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido