Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study
Author:
Funder
National Health and Medical Research Council
University of Melbourne
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference21 articles.
1. Current use of noninvasive prenatal testing in Europe, Australia and the USA: a graphical presentation;Gadsbøll;Acta Obstet Gynecol Scand,2020
2. State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study;Lindquist;Ultrasound Obstet Gynecol,2020
3. ISUOG updated consensus statement on the impact of cfDNA aneuploidy testing on screening policies and prenatal ultrasound practice;Salomon;Ultrasound Obstet Gynecol,2017
4. Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis;Grande;Ultrasound Obstet Gynecol,2015
5. Cut-off value of nuchal translucency as indication for chromosomal microarray analysis;Maya;Ultrasound Obstet Gynecol,2017
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3. Is Nuchal Translucency of 3.0–3.4 mm an Indication for cfDNA Testing or Microarray? – A Multicenter Retrospective Clinical Cohort Study;Fetal Diagnosis and Therapy;2024
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