Laboratorium Specialist in Clinical Genetics
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Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review.
Social and medical need for whole genome high resolution NIPT.
Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?
Is carriership of a balanced translocation or inversion an indication for non-invasive prenatal testing?
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands
Cytogenetic Confirmation of a Positive NIPT Result: Evidence-Based Choice Between Chorionic Villus Sampling and Amniocentesis Depending on Chromosome Aberration