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Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
Van Den Bogaert, Kris; Lannoo, Lore; Brison, Nathalie; Gatinois, Vincent; Baetens, Machteld; Blaumeiser, Bettina; Boemer, François; Bourlard, Laura; Bours, Vincent; De Leener, Anne; De Rademaeker, Marjan; Désir, Julie; Dheedene, Annelies; Duquenne, Armelle; Fieremans, Nathalie; Fieuw, Annelies; Gatot, Jean-Stéphane; Grisart, Bernard; Janssens, Katrien; Janssens, Sandra; Lederer, Damien; Marichal, Axel; Menten, Björn; Meunier, Colombine; Palmeira, Leonor; Pichon, Bruno; Sammels, Eva; Smits, Guillaume; Sznajer, Yves; Vantroys, Elise; Devriendt, Koenraad; Vermeesch, Joris Robert.
Afiliación
  • Van Den Bogaert K; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
  • Lannoo L; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
  • Brison N; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
  • Gatinois V; Center for Human Genetics, University Hospitals Leuven-KU Leuven, Leuven, Belgium.
  • Baetens M; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
  • Blaumeiser B; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Boemer F; Center for Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
  • Bourlard L; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Bours V; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • De Leener A; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • De Rademaeker M; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
  • Désir J; Center for Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
  • Dheedene A; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Duquenne A; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Fieremans N; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
  • Fieuw A; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
  • Gatot JS; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Grisart B; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Janssens K; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Janssens S; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Lederer D; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Marichal A; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
  • Menten B; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Meunier C; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Palmeira L; Center for Medical Genetics, University Hospital Ghent, Ghent, Belgium.
  • Pichon B; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Sammels E; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Smits G; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Sznajer Y; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Vantroys E; Center for Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Devriendt K; Center for Human Genetics, Université Catholique de Louvain, Brussels, Belgium.
  • Vermeesch JR; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
Genet Med ; 23(6): 1137-1142, 2021 06.
Article en En | MEDLINE | ID: mdl-33564150
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Trastornos de los Cromosomas / Pruebas Prenatales no Invasivas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Bélgica
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Trastornos de los Cromosomas / Pruebas Prenatales no Invasivas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Bélgica