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Human Mutation|December 16, 2014
Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidiesDiane Van Opstal, Femke de Vries, Lutgarde Govaerts, et al.
Prenatal Diagnosis|April 22, 2026
Impact of Maternal Body Mass Index (BMI) on the Performance of Non-Invasive Prenatal Testing (NIPT)Kristina Valovicova, Marike Polak, Sophie Ottema, et al.
The Journal of Biological Chemistry|July 13, 2004
Translational control of putative protooncogene Nm23-M2 by cytokines via phosphoinositide 3-kinase signalingMarieke Joosten, Montserrat Blázquez-Domingo, Fokke Lindeboom, et al.
Biomarkers in Medicine|July 15, 2016
Clinical experience of unexpected findings in prenatal array testingMarieke Joosten, Karin Em Diderich, Diane Van Opstal, et al.
European Journal of Medical Genetics|September 14, 2023
The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosisKarin E M Diderich, Jasmijn E Klapwijk, Vyne van der Schoot, et al.
Prenatal Diagnosis|February 11, 2024
The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort studyGeerke M Eggenhuizen, Attie T J I Go, Zoë Sauter, et al.
Journal of Clinical Medicine|August 4, 2015
The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal TestingSam Riedijk, Karin E M Diderich, Sanne L van der Steen, et al.
Molecular Cytogenetics|March 15, 2012
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalitiesMalgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, et al.
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