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Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Muys, Joke; Jacquemyn, Yves; Blaumeiser, Bettina; Bourlard, Laura; Brison, Nathalie; Bulk, Saskia; Chiarappa, Patrizia; De Leener, Anne; De Rademaeker, Marjan; Désir, Julie; Destrée, Anne; Devriendt, Koenraad; Dheedene, Annelies; Duquenne, Armelle; Fieuw, Annelies; Fransen, Erik; Gatot, Jean-Stéphane; Jamar, Mauricette; Janssens, Sandra; Kerstjens, Jorien; Keymolen, Kathelijn; Lederer, Damien; Menten, Björn; Pichon, Bruno; Rombout, Sonia; Sznajer, Yves; Van Den Bogaert, Ann; Van Den Bogaert, Kris; Vermeesch, Joris; Janssens, Katrien.
Afiliación
  • Muys J; Department of Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Jacquemyn Y; Center for Medical Genetics, Universiteit Antwerpen, Antwerpen, Belgium.
  • Blaumeiser B; Department of Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Bourlard L; ASTARC and Global Health Institute, Universiteit Antwerpen, Antwerpen, Belgium.
  • Brison N; Department of Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Bulk S; Center for Medical Genetics, Universiteit Antwerpen, Antwerpen, Belgium.
  • Chiarappa P; Center for Medical Genetics, Université Libre de Bruxelles, Bruxelles, Belgium.
  • De Leener A; Center for Medical Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
  • De Rademaeker M; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liege, Belgium.
  • Désir J; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Destrée A; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Devriendt K; Department of Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Dheedene A; Center for Medical Genetics, Université Libre de Bruxelles, Bruxelles, Belgium.
  • Duquenne A; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Gosselies, Belgium.
  • Fieuw A; Center for Medical Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
  • Fransen E; Center for Medical Genetics, Universiteit Gent, Gent, Belgium.
  • Gatot JS; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Jamar M; Center for Medical Genetics, Vrije Universiteit Brussel, Brussel, Belgium.
  • Janssens S; Center for Medical Genetics, Universiteit Antwerpen, Antwerpen, Belgium.
  • Kerstjens J; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liege, Belgium.
  • Keymolen K; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liege, Belgium.
  • Lederer D; Center for Medical Genetics, Universiteit Gent, Gent, Belgium.
  • Menten B; Faculty for Medical Sciences, Rijksuniversteit Groningen, Groningen, The Netherlands.
  • Pichon B; Center for Medical Genetics, Vrije Universiteit Brussel, Brussel, Belgium.
  • Rombout S; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Gosselies, Belgium.
  • Sznajer Y; Center for Medical Genetics, Universiteit Gent, Gent, Belgium.
  • Van Den Bogaert A; Center for Medical Genetics, Université Libre de Bruxelles, Bruxelles, Belgium.
  • Van Den Bogaert K; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Gosselies, Belgium.
  • Vermeesch J; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Janssens K; Center for Medical Genetics, Vrije Universiteit Brussel, Brussel, Belgium.
Prenat Diagn ; 40(10): 1272-1283, 2020 09.
Article en En | MEDLINE | ID: mdl-32436253
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Resultado del Embarazo / Variaciones en el Número de Copia de ADN País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2020 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Resultado del Embarazo / Variaciones en el Número de Copia de ADN País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2020 Tipo del documento: Article