Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital.

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Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41598-019-44018-4
P932PMC publication ID6533246
P698PubMed publication ID31123326

P2093author name stringJing 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
P2860cites workNoninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012Q22242878
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic reviewQ24649106
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative studyQ30414408
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 GenomicsQ34535626
Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicismQ34649324
Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysisQ35552815
Bioinformatics characterization of differential proteins in serum of mothers carrying Down syndrome fetuses: combining bioinformatics and ELISA.Q35990381
Prenatal screening methods for aneuploidiesQ36783335
Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature reviewQ37798015
Practice Bulletin No. 163: Screening for Fetal AneuploidyQ38759116
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 biologyQ41609597
Fetal loss rate and associated risk factors after amniocentesis, chorionic villus sampling and fetal blood samplingQ44174820
Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national auditQ44733231
Ultrasonographically detectable markers of fetal chromosomal abnormalitiesQ44938554
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 factorsQ46446186
Cell-free DNA analysis for noninvasive examination of trisomyQ46784231
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratoryQ47794797
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 serumQ57075132
Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospitalQ57177380
Dependence of maternal serum [AFP]/[hCG] median ratios on age of gestation: comparison of trisomy 21 to euploid pregnanciesQ84583884
Noninvasive Prenatal Screening for Fetal Sex Chromosome Aneuploidies at Two Next-Generation Sequencing PlatformsQ91132124
[Fetal loss after amniocentesis and chorionic villus sampling in Iceland]Q95566303
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)7767
P577publication date2019-05-23
P1433published inScientific ReportsQ2261792
P1476titleClinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital.
P478volume9

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cites work (P2860)
Q92340995A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Q90435963Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience

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