review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.ATG.2012.04.001 |
P8608 | Fatcat ID | release_22ieszaotncnbkyill6he26qiu |
P932 | PMC publication ID | 5121212 |
P698 | PubMed publication ID | 27896047 |
P5875 | ResearchGate publication ID | 257744169 |
P2093 | author name string | Philippos C Patsalis | |
P2860 | cites work | Detection of aneuploidy with digital polymerase chain reaction | Q48567144 |
MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21. | Q51340074 | ||
Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome | Q56765605 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
Systematic Search for Placental DNA-Methylation Markers on Chromosome 21: Toward a Maternal Plasma-Based Epigenetic Test for Fetal Trisomy 21 | Q58029321 | ||
Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational age | Q72788466 | ||
Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma | Q77372981 | ||
Detection of fetal RHD-specific sequences in maternal plasma | Q77429872 | ||
ACOG Committee Opinion No. 360: Sex selection | Q79701094 | ||
??? | Q94720111 | ||
Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic Review | Q22241933 | ||
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs) | Q24655589 | ||
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data | Q24810415 | ||
Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection | Q33268343 | ||
Epigenetic-genetic chromosome dosage approach for fetal trisomy 21 detection using an autosomal genetic reference marker | Q33797671 | ||
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study | Q34029044 | ||
Detection of the placental epigenetic signature of the maspin gene in maternal plasma. | Q34078379 | ||
Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21. | Q34168875 | ||
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study | Q34482155 | ||
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies | Q35249607 | ||
Digital PCR for the molecular detection of fetal chromosomal aneuploidy | Q35916813 | ||
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies | Q37164146 | ||
The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis | Q37306246 | ||
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 | ||
Human aneuploidy: incidence, origin, and etiology | Q41202582 | ||
P921 | main subject | Down syndrome | Q47715 |
P304 | page(s) | 3-8 | |
P577 | publication date | 2012-05-26 | |
P1433 | published in | Applied & translational genomics | Q27725407 |
P1476 | title | A new method for non-invasive prenatal diagnosis of Down syndrome using MeDIP real time qPCR. | |
P478 | volume | 1 |
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