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Non-invasive prenatal diagnosis for translocation carriers
Does non-invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands?
Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders
Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the Netherlands