Clinical experience with non‐invasive prenatal screening for single‐gene disorders
Author:
Affiliation:
1. Natera, Inc., San Carlos CA USA
2. Baylor Genetics Houston TX USA
3. Baylor College of Medicine Houston TX USA
4. Department of Genetics and Genome Sciences University of Connecticut Health Center Farmington CT USA
Publisher
Wiley
Subject
Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.23756
Reference21 articles.
1. Presence of fetal DNA in maternal plasma and serum
2. DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study
3. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study
4. Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing
5. Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort
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