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Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
Dommering, Charlotte J; Henneman, Lidewij; van der Hout, Annemarie H; Jonker, Marianne A; Tops, Carli M J; van den Ouweland, Ans M W; van der Luijt, Rob B; Mensenkamp, Arjen R; Hogervorst, Frans B L; Redeker, Egbert J W; de Die-Smulders, Christine E M; Moll, Annette C; Meijers-Heijboer, Hanne.
Afiliación
  • Dommering CJ; Department of Clinical Genetics, VU University Medical Center, PO Box 7057, 1007 MB, Amsterdam, The Netherlands. cj.dommering@vumc.nl.
  • Henneman L; Department of Clinical Genetics, VU University Medical Center, PO Box 7057, 1007 MB, Amsterdam, The Netherlands.
  • van der Hout AH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Jonker MA; Department of Mathematics, Faculty of Sciences, VU University, Amsterdam, The Netherlands.
  • Tops CM; Department for Health Evidence, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van den Ouweland AM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • van der Luijt RB; Department Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Mensenkamp AR; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Hogervorst FB; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Redeker EJ; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • de Die-Smulders CE; Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Moll AC; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Meijers-Heijboer H; Department of Ophthalmology, VU University Medical Center, Amsterdam, The Netherlands.
Fam Cancer ; 16(2): 271-277, 2017 04.
Article en En | MEDLINE | ID: mdl-27826806
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Retinoblastoma / Síndromes Neoplásicos Hereditarios / Pruebas Genéticas / Genes de Retinoblastoma / Detección Precoz del Cáncer Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies País/Región como asunto: Europa Idioma: En Revista: Fam Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article
Texto completo
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XML
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Retinoblastoma / Síndromes Neoplásicos Hereditarios / Pruebas Genéticas / Genes de Retinoblastoma / Detección Precoz del Cáncer Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies País/Región como asunto: Europa Idioma: En Revista: Fam Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article