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Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Van Opstal, Diane; van Maarle, Merel C; Lichtenbelt, Klaske; Weiss, Marjan M; Schuring-Blom, Heleen; Bhola, Shama L; Hoffer, Mariette J V; Huijsdens-van Amsterdam, Karin; Macville, Merryn V; Kooper, Angelique J A; Faas, Brigitte H W; Govaerts, Lutgarde; Tan-Sindhunata, Gita M; den Hollander, Nicolette; Feenstra, Ilse; Galjaard, Robert-Jan H; Oepkes, Dick; Ghesquiere, Stijn; Brouwer, Rutger W W; Beulen, Lean; Bollen, Sander; Elferink, Martin G; Straver, Roy; Henneman, Lidewij; Page-Christiaens, Godelieve C; Sistermans, Erik A.
Afiliación
  • Van Opstal D; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van Maarle MC; Department of Clinical Genetics, Academic Medical Center, Amsterdam, Amsterdam, The Netherlands.
  • Lichtenbelt K; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Weiss MM; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Schuring-Blom H; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Bhola SL; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Huijsdens-van Amsterdam K; Department of Clinical Genetics, Academic Medical Center, Amsterdam, Amsterdam, The Netherlands.
  • Macville MV; Department of Clinical Genetics, Maastricht UMC+, Maastricht, The Netherlands.
  • Kooper AJA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Faas BHW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Govaerts L; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Tan-Sindhunata GM; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • den Hollander N; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Feenstra I; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Galjaard RH; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Oepkes D; Department of Obstetrics, Leiden University Medical Center, Leiden, The Netherlands.
  • Ghesquiere S; Department of Clinical Genetics, Maastricht UMC+, Maastricht, The Netherlands.
  • Brouwer RWW; Erasmus Center for Biomics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Beulen L; Department of Obstetrics and Gynaecology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Bollen S; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Elferink MG; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Straver R; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Henneman L; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Page-Christiaens GC; Department of Obstetrics and Gynaecology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Sistermans EA; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
Genet Med ; 20(5): 480-485, 2018 04.
Article en En | MEDLINE | ID: mdl-29121006
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Trisomía / Pruebas Genéticas / Aberraciones Cromosómicas / Trastornos de los Cromosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Trisomía / Pruebas Genéticas / Aberraciones Cromosómicas / Trastornos de los Cromosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos