scholarly article | Q13442814 |
P356 | DOI | 10.1002/PD.4777 |
P8608 | Fatcat ID | release_2iduex4n5fb2bjd4bvzbob4pye |
P698 | PubMed publication ID | 26774010 |
P50 | author | Brigitte H. W. Faas | Q130284899 |
P2093 | author name string | Kornelia Neveling | |
Ingrid Gomes | |||
Simone van den Heuvel | |||
Lean Beulen | |||
Hanneke Mieloo | |||
Djie Tjwan Thung | |||
Ellen Kater-Baats | |||
Irma Derks-Prinsen | |||
Wendy van Rens-Buijsman | |||
P2860 | cites work | DNA Sequencing versus Standard Prenatal Aneuploidy Screening | Q22250872 |
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma | Q33360224 | ||
Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing | Q33665399 | ||
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing | Q34256640 | ||
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
Feasibility study of semiconductor sequencing for noninvasive prenatal detection of fetal aneuploidy | Q34567793 | ||
Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis | Q35552815 | ||
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy | Q36406163 | ||
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 | ||
Introducing WISECONDOR for noninvasive prenatal diagnostics | Q38211988 | ||
Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories | Q38262952 | ||
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18. | Q40028555 | ||
Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipuncture | Q43804527 | ||
Noninvasive detection of a balanced fetal translocation from maternal plasma | Q44233638 | ||
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors | Q46446186 | ||
Successful noninvasive trisomy 18 detection using single molecule sequencing. | Q46986331 | ||
Size distributions of maternal and fetal DNA in maternal plasma. | Q47432593 | ||
Theoretical performance of non-invasive prenatal testing for chromosome imbalances using counting of cell-free DNA fragments in maternal plasma. | Q50674465 | ||
Circulating fetal cell-free DNA fractions differ in autosomal aneuploidies and monosomy X. | Q51163080 | ||
Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection. | Q51514162 | ||
Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21. | Q53063252 | ||
Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection. | Q53094776 | ||
Delivering noninvasive prenatal testing in a clinical setting using semiconductor sequencing platform. | Q53516393 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells | Q57079533 | ||
P433 | issue | 3 | |
P304 | page(s) | 216-223 | |
P577 | publication date | 2016-01-15 | |
P1433 | published in | Prenatal Diagnosis | Q15760059 |
P1476 | title | Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations | |
P478 | volume | 36 |
Q33845848 | Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies | cites work | P2860 |
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