Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.
about
Male microchimerism in the human female brainPlasmodium falciparum histones induce endothelial proinflammatory response and barrier dysfunctionCongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guidelineNoninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal bloodMethodology for detecting trace amounts of microchimeric DNA from peripheral murine white blood cells by real-time PCRQuantitative analysis of DNA levels in maternal plasma in normal and Down syndrome pregnanciesPlacental origins of adverse pregnancy outcomes: potential molecular targets: an Executive Workshop Summary of the Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentNon-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsTracking fetal development through molecular analysis of maternal biofluidsExtracellular nucleic acids in maternal circulation as potential biomarkers for placental insufficiencyMolecular Regulation of Parturition: The Role of the Decidual ClockMethylation of cell-free circulating DNA in the diagnosis of cancerCell-free fetal DNA in maternal plasma: an important advance to link fetal genetics to obstetric ultrasoundTelegony, the sire effect and non-mendelian inheritance mediated by spermatozoa: a historical overview and modern mechanistic speculationsThe forensiX evidence collection tube and its impact on DNA preservation and recoveryFAST-SeqS: a simple and efficient method for the detection of aneuploidy by massively parallel sequencingNoninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNAImplementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yieldSensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statisticsThe accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis.Routes to improving the reliability of low level DNA analysis using real-time PCR.Genotyping fetal DNA by non-invasive means: extraction from maternal plasma.Quantitation of genomic DNA in plasma and serum samples: higher concentrations of genomic DNA found in serum than in plasma.MALDI-TOF mass spectrometry for quantitative, specific, and sensitive analysis of DNA and RNA.A uniform genomic minor histocompatibility antigen typing methodology and database designed to facilitate clinical applications.Hypermethylation of RASSF1A in human and rhesus placentas.Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.A rapid and accurate approach to identify single nucleotide polymorphisms of mitochondrial DNA using MALDI-TOF mass spectrometry.Host-derived smooth muscle cells accumulate in cardiac allografts: role of inflammation and monocyte chemoattractant protein 1.Safe fetal platelet genotyping: new developments.Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing.Diagnosing schistosomiasis by detection of cell-free parasite DNA in human plasma.Abnormal DNA methylation as a cell-free circulating DNA biomarker for colorectal cancer detection: A review of literature.Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testingImproving enrichment of circulating fetal DNA for genetic testing: size fractionation followed by whole gene amplificationLymphotropic polyomavirus is detected in peripheral blood from immunocompromised and healthy subjectsFetal cells in the maternal circulation: feasibility for prenatal diagnosis.Rapid prenatal diagnosis of trisomy 21 by real-time quantitative polymerase chain reaction with amplification of small tandem repeats and S100B in chromosome 21Microchimerism: implications for autoimmune disease.New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.
P2860
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P2860
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@ast
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@en
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@nl
type
label
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@ast
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@en
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@nl
prefLabel
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@ast
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@en
Quantitative analysis of fetal ...... oninvasive prenatal diagnosis.
@nl
P2093
P356
P1476
Quantitative analysis of fetal ...... noninvasive prenatal diagnosis
@en
P2093
Johnson PJ
Wainscoat JS
P304
P356
10.1086/301800
P407
P50
P577
1998-04-01T00:00:00Z