| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Beryl R Benacerraf | Q89950977 |
| P2093 | author name string | Simcha Yagel | |
| Jan M M van Lith | |||
| P2860 | cites work | Noninvasive Prenatal Detection of Fetal Trisomy 18 by Epigenetic Allelic Ratio Analysis in Maternal Plasma: Theoretical and Empirical Considerations | Q58029492 |
| Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
| Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma | Q28314918 | ||
| Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics | Q28752377 | ||
| Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection | Q33268343 | ||
| Microfluidic digital PCR enables rapid prenatal diagnosis of fetal aneuploidy | Q33980278 | ||
| Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
| Rapid clearance of fetal DNA from maternal plasma | Q34388637 | ||
| First- and second-trimester evaluation of risk for Down syndrome | Q34643774 | ||
| Role of second-trimester genetic sonography after Down syndrome screening | Q36776424 | ||
| Time to reconsider our approach to echogenic intracardiac focus and choroid plexus cysts | Q37119113 | ||
| Impact of first-trimester aneuploidy screening in a high-risk population | Q37611397 | ||
| Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach. | Q39904859 | ||
| Synergy of total PLAC4 RNA concentration and measurement of the RNA single-nucleotide polymorphism allelic ratio for the noninvasive prenatal detection of trisomy 21. | Q39906674 | ||
| Contingent screening for Down syndrome--results from the FaSTER trial. | Q46781339 | ||
| First-trimester or second-trimester screening, or both, for Down's syndrome | Q46799629 | ||
| Analysis of the size distributions of fetal and maternal cell-free DNA by paired-end sequencing | Q47427812 | ||
| Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21. | Q53063252 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation | Q57523616 | ||
| P433 | issue | 3 | |
| P921 | main subject | Down syndrome | Q47715 |
| P304 | page(s) | 231-234 | |
| P577 | publication date | 2011-02-10 | |
| P1433 | published in | Prenatal Diagnosis | Q15760059 |
| P1476 | title | Current controversies in prenatal diagnosis 2: Down syndrome screening: is ultrasound better than cell-free nucleic acids in maternal blood? | |
| P478 | volume | 31 |
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