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The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Muys, Joke; Blaumeiser, Bettina; Jacquemyn, Yves; Bandelier, Claude; Brison, Nathalie; Bulk, Saskia; Chiarappa, Patrizia; Courtens, Winnie; De Leener, Anne; De Rademaeker, Marjan; Désir, Julie; Destrée, Anne; Devriendt, Koenraad; Dheedene, Annelies; Fieuw, Annelies; Fransen, Erik; Gatot, Jean-Stéphane; Holmgren, Philip; Jamar, Mauricette; Janssens, Sandra; Keymolen, Kathelijn; Lederer, Damien; Menten, Björn; Meuwissen, Marije; Parmentier, Benoit; Pichon, Bruno; Rombout, Sonia; Sznajer, Yves; Van Den Bogaert, Ann; Van Den Bogaert, Kris; Vanakker, Olivier; Vermeesch, Joris; Janssens, Katrien.
Afiliación
  • Muys J; Department of Obstetrics and Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Blaumeiser B; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Jacquemyn Y; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Bandelier C; Department of Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
  • Brison N; Department of Obstetrics and Gynaecology, University Hospital Antwerp, Edegem, Belgium.
  • Bulk S; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Chiarappa P; Center for Medical Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
  • Courtens W; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • De Leener A; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • De Rademaeker M; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Désir J; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Destrée A; Department of Medical Genetics, University Hospital Antwerp, Edegem, Belgium.
  • Devriendt K; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Dheedene A; Center for Medical Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Fieuw A; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Fransen E; Center for Medical Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
  • Gatot JS; Center for Medical Genetics, Universiteit Gent, Ghent, Belgium.
  • Holmgren P; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Jamar M; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Janssens S; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Keymolen K; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Lederer D; Center for Medical Genetics, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Menten B; Center for Medical Genetics, Universiteit Gent, Ghent, Belgium.
  • Meuwissen M; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Parmentier B; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Pichon B; Center for Medical Genetics, Universiteit Gent, Ghent, Belgium.
  • Rombout S; Center for Medical Genetics, Universiteit Antwerpen, Antwerp, Belgium.
  • Sznajer Y; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Van Den Bogaert A; Center for Medical Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Van Den Bogaert K; Center for Medical Genetics, Institut de Pathologie et de Génétique Gosselies, Charleroi, Belgium.
  • Vanakker O; Center for Medical Genetics, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Vermeesch J; Center for Medical Genetics, Vrije Universiteit Brussel, Brussels, Belgium.
  • Janssens K; Center for Medical Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
Prenat Diagn ; 38(13): 1120-1128, 2018 12.
Article en En | MEDLINE | ID: mdl-30334587
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Aberraciones Cromosómicas / Análisis por Micromatrices / Variaciones en el Número de Copia de ADN / Haploinsuficiencia Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2018 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: Anomalías Congénitas / Aberraciones Cromosómicas / Análisis por Micromatrices / Variaciones en el Número de Copia de ADN / Haploinsuficiencia Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Prenat Diagn Año: 2018 Tipo del documento: Article País de afiliación: Bélgica