scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1020911194 |
P356 | DOI | 10.1186/S13039-016-0213-4 |
P932 | PMC publication ID | 4709980 |
P698 | PubMed publication ID | 26759606 |
P5875 | ResearchGate publication ID | 290244542 |
P50 | author | Wei Wang | Q110785130 |
P2093 | author name string | Lili Zhang | |
Haibo Li | |||
Hong Li | |||
Qin Zhang | |||
Ting Wang | |||
Minjuan Liu | |||
Jie Ding | |||
Quanze He | |||
Ping Wen | |||
Cong Shen | |||
Jingjing Xiang | |||
Chengying Duan | |||
P2860 | cites work | Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management | Q27324761 |
Copy-number variation and false positive prenatal aneuploidy screening results | Q30643919 | ||
Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing | Q33760408 | ||
High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma | Q34618332 | ||
Noninvasive prenatal molecular karyotyping from maternal plasma | Q34683906 | ||
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 | ||
Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma | Q44554684 | ||
A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing | Q45049473 | ||
Noninvasive prenatal testing: the paradigm is shifting rapidly | Q48240788 | ||
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma. | Q50955444 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting | Q83395075 | ||
Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies | Q85274591 | ||
P304 | page(s) | 3 | |
P577 | publication date | 2016-01-12 | |
P1433 | published in | Molecular Cytogenetics | Q15761790 |
P1476 | title | Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing | |
P478 | volume | 9 |
Q90447136 | Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma |
Q38860845 | Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y. |
Q64969403 | Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies. |
Q38867682 | Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood |
Q92062150 | Noninvasive prenatal testing detects microdeletion abnormalities of fetal chromosome 15 |
Q91790685 | Sequencing Shorter cfDNA Fragments Decreases the False Negative Rate of Non-invasive Prenatal Testing |
Q91873307 | Whole exome sequencing aids the diagnosis of Simpson-Golabi-Behmel syndrome in two male fetuses |
Q55427016 | Why do patients decline amniocentesis? Analysis of factors influencing the decision to refuse invasive prenatal testing. |
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