Comment on “The clinical utility of genome-wide non invasive prenatal screening”
Author:
Affiliation:
1. TOMA, Advanced Biomedical Assays S.p.A; Busto Arsizio Varese Italy
2. Department of Genetics and Genome Sciences; University of Connecticut Health Center; Farmington CT USA
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference22 articles.
1. The clinical utility of genome-wide non invasive prenatal screening;Fiorentino;Prenat Diagn,2017
2. Implications of fetoplacental mosaicism on cell-free DNA testing: a review of a common biological phenomenon;Grati;Ultrasound Obstet Gynecol,2016
3. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications;Ferreira;Prenat Diagn,2016
4. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012
5. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies;Grati;Prenat Diagn,2015
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1. “RATs”: Rare Autosomal Trisomies and Their Relevance in cfDNA Testing;Prenatal Diagnostic Testing for Genetic Disorders;2023
2. Confirmation rate of cell free DNA screening for sex chromosomal abnormalities according to the method of confirmatory testing;Prenatal Diagnosis;2020-09-02
3. Rare autosomal trisomies: comparison of detection through cell‐free DNA analysis and direct chromosome preparation of chorionic villus samples;Ultrasound in Obstetrics & Gynecology;2019-09-03
4. Expanding the indications for cell-free DNA in the maternal circulation: clinical considerations and implications;American Journal of Obstetrics and Gynecology;2019-06
5. DEGUM, ÖGUM, SGUM and FMF Germany Recommendations for the Implementation of First-Trimester Screening, Detailed Ultrasound, Cell-Free DNA Screening and Diagnostic Procedures;Ultraschall in der Medizin - European Journal of Ultrasound;2018-07-12
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