scholarly article | Q13442814 |
P2093 | author name string | Eva Pazourkova | |
Marie Korabecna | |||
Barbora Vesela | |||
Iveta Zednikova | |||
Sona Lassakova | |||
P2860 | cites work | High-throughput, non-invasive prenatal testing for fetal rhesus D status in RhD-negative women: a systematic review and meta-analysis | Q64243238 |
Use of bi-allelic insertion/deletion polymorphisms as a positive control for fetal genotyping in maternal blood: first clinical experience | Q79362850 | ||
On the Determination of Uncertainty and Limit of Detection in Label-Free Biosensors | Q89292149 | ||
Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia | Q90467894 | ||
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination | Q30987480 | ||
Wiskott-Aldrich syndrome: a comprehensive review | Q33406620 | ||
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Performance of non-invasive prenatal testing when fetal cell-free DNA is absent | Q34996829 | ||
Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis | Q35209735 | ||
Performance of Droplet Digital PCR in Non-Invasive Fetal RHD Genotyping - Comparison with a Routine Real-Time PCR Based Approach | Q35839919 | ||
A multifactorial relationship exists between total circulating cell-free DNA levels and maternal BMI | Q36205202 | ||
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Determining lower limits of detection of digital PCR assays for cancer-related gene mutations | Q37456162 | ||
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Cell-Free Fetal DNA Testing for Prenatal Diagnosis | Q38958956 | ||
Quantification of free fetal DNA in multiple pregnancies and relationship with chorionicity | Q39727263 | ||
Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia | Q40350792 | ||
X-chromosomal 21-indel marker panel in German and Baltic populations | Q40747985 | ||
Effects of Maternal and Fetal Characteristics on Cell-Free Fetal DNA Fraction in Maternal Plasma | Q40950309 | ||
Noninvasive prenatal diagnosis of early onset primary dystonia I in maternal plasma | Q43257809 | ||
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Measurement of fetal fraction in cell-free DNA from maternal plasma using a panel of insertion/deletion polymorphisms | Q47130174 | ||
X-linked insertion/deletion polymorphisms: forensic applications of a 33-markers panel | Q47399004 | ||
Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report | Q48004844 | ||
Non-invasive prenatal diagnosis of monogenic disorders: an optimized protocol using MEMO qPCR with miniSTR as internal control. | Q50631143 | ||
Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCR. | Q52610351 | ||
Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. | Q54574187 | ||
Non-invasive fetal sex diagnosis in plasma of early weeks pregnants using droplet digital PCR. | Q55418615 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
A method for the analysis of 32 X chromosome insertion deletion polymorphisms in a single PCR | Q57083810 | ||
Cell-Free Fetal DNA in Maternal Plasma during Physiological Single Male Pregnancies: Methodology Issues and Kinetics | Q57557794 | ||
Effective Fetal Epigenetic Biomarkers for Noninvasive Fetal Trisomy 21 Detections | Q58580064 | ||
P433 | issue | 1 | |
P304 | page(s) | 20036 | |
P577 | publication date | 2020-11-18 | |
P1433 | published in | Scientific Reports | Q2261792 |
P1476 | title | Detection of cell-free foetal DNA fraction in female-foetus bearing pregnancies using X-chromosomal insertion/deletion polymorphisms examined by digital droplet PCR | |
P478 | volume | 10 |
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