scholarly article | Q13442814 |
P356 | DOI | 10.1586/14737159.2014.919855 |
P698 | PubMed publication ID | 24831532 |
P2093 | author name string | Erik A Sistermans | |
Marcel J T Reinders | |||
Roy Straver | |||
P2860 | cites work | DNA Sequencing versus Standard Prenatal Aneuploidy Screening | Q22250872 |
Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination | Q30987480 | ||
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma | Q36595101 | ||
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme. | Q37631891 | ||
Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood | Q44645735 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
P433 | issue | 5 | |
P304 | page(s) | 513-515 | |
P577 | publication date | 2014-05-16 | |
P1433 | published in | Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare | Q15756305 |
P1476 | title | Introducing WISECONDOR for noninvasive prenatal diagnostics | |
P478 | volume | 14 |
Q33845848 | Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies |
Q36312158 | Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing |
Q38728695 | Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration. |
Q37412801 | Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory |
Q36184534 | Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening |
Q26764809 | Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues |
Q48274405 | The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies |
Q38410274 | Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations |
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