Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing

scientific article

Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1020911194
P356DOI10.1186/S13039-016-0213-4
P932PMC publication ID4709980
P698PubMed publication ID26759606
P5875ResearchGate publication ID290244542

P50authorWei WangQ110785130
P2093author name stringLili Zhang
Haibo Li
Hong Li
Qin Zhang
Ting Wang
Minjuan Liu
Jie Ding
Quanze He
Ping Wen
Cong Shen
Jingjing Xiang
Chengying Duan
P2860cites workNoninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementQ27324761
Copy-number variation and false positive prenatal aneuploidy screening resultsQ30643919
Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencingQ33760408
High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasmaQ34618332
Noninvasive prenatal molecular karyotyping from maternal plasmaQ34683906
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasmaQ37010246
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 plasmaQ44554684
A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencingQ45049473
Noninvasive prenatal testing: the paradigm is shifting rapidlyQ48240788
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.Q50955444
Presence of fetal DNA in maternal plasma and serumQ57075132
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical settingQ83395075
Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidiesQ85274591
P304page(s)3
P577publication date2016-01-12
P1433published inMolecular CytogeneticsQ15761790
P1476titleDetection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing
P478volume9

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cites work (P2860)
Q90447136Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma
Q38860845Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.
Q64969403Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies.
Q38867682Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood
Q92062150Noninvasive prenatal testing detects microdeletion abnormalities of fetal chromosome 15
Q91790685Sequencing Shorter cfDNA Fragments Decreases the False Negative Rate of Non-invasive Prenatal Testing
Q91873307Whole exome sequencing aids the diagnosis of Simpson-Golabi-Behmel syndrome in two male fetuses
Q55427016Why do patients decline amniocentesis? Analysis of factors influencing the decision to refuse invasive prenatal testing.

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