scholarly article | Q13442814 |
P2093 | author name string | Jing Cheng | |
Qian Zhu | |||
Yuan Luo | |||
Ting Bai | |||
Sha Liu | |||
Hongqian Liu | |||
Jianlong Liu | |||
Xiang Wei | |||
Yunyun Liu | |||
Lingling Xing | |||
Tianyu Xia | |||
Cechuan Deng | |||
Xiaosha Jing | |||
Zhunduo Li | |||
P2860 | cites work | Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 | Q22242878 |
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review | Q24649106 | ||
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study | Q30414408 | ||
Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y. | Q34340985 | ||
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics | Q34535626 | ||
Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism | Q34649324 | ||
Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis | Q35552815 | ||
Bioinformatics characterization of differential proteins in serum of mothers carrying Down syndrome fetuses: combining bioinformatics and ELISA. | Q35990381 | ||
Prenatal screening methods for aneuploidies | Q36783335 | ||
Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review | Q37798015 | ||
Practice Bulletin No. 163: Screening for Fetal Aneuploidy | Q38759116 | ||
Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies. | Q41566460 | ||
Fetal sex chromosome testing by maternal plasma DNA sequencing: clinical laboratory experience and biology | Q41609597 | ||
Fetal loss rate and associated risk factors after amniocentesis, chorionic villus sampling and fetal blood sampling | Q44174820 | ||
Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national audit | Q44733231 | ||
Ultrasonographically detectable markers of fetal chromosomal abnormalities | Q44938554 | ||
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA. | Q45026733 | ||
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 | ||
Cell-free DNA analysis for noninvasive examination of trisomy | Q46784231 | ||
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory | Q47794797 | ||
Maternal mosaicism of sex chromosome causes discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing. | Q50551782 | ||
Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction. | Q51114145 | ||
Implications of fetoplacental mosaicism on cell-free DNA testing: a review of a common biological phenomenon. | Q53091843 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital | Q57177380 | ||
Dependence of maternal serum [AFP]/[hCG] median ratios on age of gestation: comparison of trisomy 21 to euploid pregnancies | Q84583884 | ||
Noninvasive Prenatal Screening for Fetal Sex Chromosome Aneuploidies at Two Next-Generation Sequencing Platforms | Q91132124 | ||
[Fetal loss after amniocentesis and chorionic villus sampling in Iceland] | Q95566303 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 7767 | |
P577 | publication date | 2019-05-23 | |
P1433 | published in | Scientific Reports | Q2261792 |
P1476 | title | Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital. | |
P478 | volume | 9 |
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