Screening for trisomies 21 and 18 in a Spanish public hospital: from the combined test to the cell-free DNA test
Author:
Affiliation:
1. Department of Obstetrics and Gynecology, Torrejon University Hospital, Torrejon de Ardoz, Madrid, Spain and
2. Clinical Analysis Laboratory of Torrejon University Hospital, Unilabs®, Madrid, Spain
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2016.1253062
Reference22 articles.
1. Screening for fetal aneuploidies at 11 to 13 weeks
2. Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal Abnormalities
3. Presence of fetal DNA in maternal plasma and serum
4. Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis
5. Diagnóstico prenatal de los defectos congénitos. Cribado de las anomalías cromosómicas (actualizada 2010). Guías de Asistencia práctica. Sociedad Española de Ginecología y Obstetricia (SEGO). Available from: http://www.gapsego.com [last accessed 30 Apr 2016]
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2. A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy X;Journal of Clinical Medicine;2022-08-15
3. Clinical performance of DNA‐based prenatal screening using single‐nucleotide polymorphisms approach in Thai women with singleton pregnancy;Molecular Genetics & Genomic Medicine;2020-04-24
4. Antenatal screening for fetal trisomies using microarray‐based cell‐free DNA testing: A systematic review and meta‐analysis;Prenatal Diagnosis;2020-03
5. Clinical and Economic Evaluation after Adopting Contingent Cell-Free DNA Screening for Fetal Trisomies in South Spain;Fetal Diagnosis and Therapy;2020
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