Potential diagnostic consequences of applying non-invasive prenatal testing: population-based study from a country with existing first-trimester screening

Noninvasive Detection of Fetal Subchromosome Abnormalities via Deep Sequencing of Maternal Plasma

(2013) Anupama Srinivasan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population

(2012) Kypros H. Nicolaides et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18

(2012) Ghalia Ashoor et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

A new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR

(2012) Philippos C Patsalis et al.   EXPERT OPINION ON BIOLOGICAL THERAPY

Combined Screening for Preeclampsia and Small for Gestational Age at 11–13 Weeks

(2012) Leona C.Y. Poon et al.   FETAL DIAGNOSIS AND THERAPY

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

(2012) Ronald J. Wapner et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing

(2012) Diana W. Bianchi et al.   OBSTETRICS AND GYNECOLOGY

Committee Opinion No. 545

(2012)   OBSTETRICS AND GYNECOLOGY

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

(2012) Lisa G. Shaffer et al.   PRENATAL DIAGNOSIS

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors

(2012) Shan Dan et al.   PRENATAL DIAGNOSIS

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

(2012) Bernhard Zimmermann et al.   PRENATAL DIAGNOSIS

DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

(2011) Glenn E. Palomaki et al.   GENETICS IN MEDICINE

Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks

(2011) Argyro Syngelaki et al.   PRENATAL DIAGNOSIS

Experiences with risk estimates for carriers of chromosomal reciprocal translocations

(2010) Alina T. Midro et al.   CLINICAL GENETICS

Prospective validation of first-trimester combined screening for trisomy 21

(2009) K. O. Kagan et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY