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Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
Barisic, Ingeborg; Boban, Ljubica; Akhmedzhanova, Diana; Bergman, Jorieke E H; Cavero-Carbonell, Clara; Grinfelde, Ieva; Materna-Kiryluk, Anna; Latos-Bielenska, Anna; Randrianaivo, Hanitra; Zymak-Zakutnya, Natalya; Sansovic, Ivona; Lanzoni, Monica; Morris, Joan K.
Afiliação
  • Barisic I; Department of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, School of Medicine, University of Zagreb, Zagreb, Croatia. Electronic address: ingeborg.barisic@kdb.hr.
  • Boban L; Department of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, School of Medicine, University of Zagreb, Zagreb, Croatia.
  • Akhmedzhanova D; OMNI-Net Ukraine and Khmelnytsky City Perinatal Center, Khmelnytsky, Ukraine.
  • Bergman JEH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Grinfelde I; Medical Genetics and Prenatal Diagnosis Clinic, Children's University Hospital, Riga, Latvia.
  • Materna-Kiryluk A; Department of Medical Genetics, Poznan University of Medical Sciences and Center for Medical Genetics GENESIS, Poznan, Poland.
  • Latos-Bielenska A; Department of Medical Genetics, Poznan University of Medical Sciences and Center for Medical Genetics GENESIS, Poznan, Poland.
  • Randrianaivo H; Registre des Malformations Congenitales de la Reunion, St Pierre, Ile de la Reunion, France.
  • Zymak-Zakutnya N; OMNI-Net Ukraine and Khmelnytsky City Perinatal Center, Khmelnytsky, Ukraine.
  • Sansovic I; Department of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, School of Medicine, University of Zagreb, Zagreb, Croatia.
  • Lanzoni M; European Commission, DG Joint Research Centre, Ispra, Italy.
  • Morris JK; Queen Mary University of London, UK.
Eur J Med Genet ; 61(9): 499-507, 2018 Sep.
Article em En | MEDLINE | ID: mdl-29753922
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudo: Diagnostic_studies / Prevalence_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudo: Diagnostic_studies / Prevalence_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article