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Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.
Duerinckx, Sarah; Désir, Julie; Perazzolo, Camille; Badoer, Cindy; Jacquemin, Valérie; Soblet, Julie; Maystadt, Isabelle; Tunca, Yusuf; Blaumeiser, Bettina; Ceulemans, Berten; Courtens, Winnie; Debray, François-Guillaume; Destree, Anne; Devriendt, Koenraad; Jansen, Anna; Keymolen, Kathelijn; Lederer, Damien; Loeys, Bart; Meuwissen, Marije; Moortgat, Stéphanie; Mortier, Geert; Nassogne, Marie-Cécile; Sekhara, Tayeb; Van Coster, Rudy; Van Den Ende, Jenny; Van der Aa, Nathalie; Van Esch, Hilde; Vanakker, Olivier; Verhelst, Helene; Vilain, Catheline; Weckhuysen, Sarah; Passemard, Sandrine; Verloes, Alain; Aeby, Alec; Deconinck, Nicolas; Van Bogaert, Patrick; Pirson, Isabelle; Abramowicz, Marc.
Afiliación
  • Duerinckx S; Institut de Recherche Interdisciplinaire en Biologie Humaine et moléculaire, Université Libre de Bruxelles, Brussels, Belgium.
  • Désir J; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Perazzolo C; Institut de Recherche Interdisciplinaire en Biologie Humaine et moléculaire, Université Libre de Bruxelles, Brussels, Belgium.
  • Badoer C; Department of Genetics, Hôpital Erasme, ULB Center of Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Jacquemin V; Institut de Recherche Interdisciplinaire en Biologie Humaine et moléculaire, Université Libre de Bruxelles, Brussels, Belgium.
  • Soblet J; Department of Genetics, Hôpital Erasme, ULB Center of Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Maystadt I; Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Université Libre de Bruxelles, Brussels, Belgium.
  • Tunca Y; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Blaumeiser B; Department of Medical Genetics, Gülhane Faculty of Medicine & Gülhane Training and Research Hospital, University of Health Sciences Turkey, Ankara, Turkey.
  • Ceulemans B; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Courtens W; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Debray FG; Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Destree A; Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Devriendt K; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Jansen A; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Keymolen K; Universitair Ziekenhuis Brussel (UZ Brussel), Centrum Medische Genetica, Universiteit Brussel (VUB), Brussels, Belgium.
  • Lederer D; Universitair Ziekenhuis Brussel (UZ Brussel), Centrum Medische Genetica, Universiteit Brussel (VUB), Brussels, Belgium.
  • Loeys B; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Meuwissen M; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Moortgat S; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Mortier G; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Nassogne MC; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Sekhara T; Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
  • Van Coster R; Centre Hospitalier CHIREC, Brussels, Belgium.
  • Van Den Ende J; Universitair Ziekenhuis Gent, Ghent, Belgium.
  • Van der Aa N; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Van Esch H; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Vanakker O; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Verhelst H; Universitair Ziekenhuis Gent, Ghent, Belgium.
  • Vilain C; Universitair Ziekenhuis Gent, Ghent, Belgium.
  • Weckhuysen S; Department of Genetics, Hôpital Erasme, ULB Center of Human Genetics, Université Libre de Bruxelles, Brussels, Belgium.
  • Passemard S; Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Université Libre de Bruxelles, Brussels, Belgium.
  • Verloes A; University and University Hospital of Antwerp, Antwerp, Belgium.
  • Aeby A; Department of Genetics, APHP, Robert Debré University Hospital, Paris, France.
  • Deconinck N; Department of Genetics, APHP, Robert Debré University Hospital, Paris, France.
  • Van Bogaert P; Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Université Libre de Bruxelles, Brussels, Belgium.
  • Pirson I; Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Université Libre de Bruxelles, Brussels, Belgium.
  • Abramowicz M; Department of Pediatrics, Centre Hospitalier Universitaire d'Angers, France.
Mol Genet Genomic Med ; 9(9): e1768, 2021 09.
Article en En | MEDLINE | ID: mdl-34402213
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Consanguinidad / Epilepsia / Genotipo / Microcefalia Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2021 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Consanguinidad / Epilepsia / Genotipo / Microcefalia Tipo de estudio: Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2021 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos