Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort

OBJECTIVE:To estimate performance of a single-nucleotide polymorphism–based noninvasive prenatal screen for fetal aneuploidy in high-risk and low-risk populations on single venopuncture. METHODS:One thousand sixty-four maternal blood samples from 7 weeks of gestation and beyond were included; 1,051...

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Veröffentlicht in:	Obstetrics and gynecology (New York. 1953) 2014-08, Vol.124 (2), p.210-218
Hauptverfasser:	Pergament, Eugene, Cuckle, Howard, Zimmermann, Bernhard, Banjevic, Milena, Sigurjonsson, Styrmir, Ryan, Allison, Hall, Megan P., Dodd, Michael, Lacroute, Phil, Stosic, Melissa, Chopra, Nikhil, Hunkapiller, Nathan, Prosen, Dennis E., McAdoo, Sallie, Demko, Zachary, Siddiqui, Asim, Hill, Matthew, Rabinowitz, Matthew
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Algorithms Aneuploidy Cell-Free System Chromosome Disorders - diagnosis Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 18 DNA - blood Down Syndrome - diagnosis Female Humans Male Middle Aged Polymorphism, Single Nucleotide Pregnancy Prenatal Diagnosis - methods Risk Factors Sensitivity and Specificity Trisomy - diagnosis Trisomy 13 Syndrome Trisomy 18 Syndrome Turner Syndrome - diagnosis Young Adult
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