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• W2024456811 startingPage "771" @default.
• W2024456811 abstract "Non-invasive prenatal testing using next generation sequencing technology with cell free fetal DNA from the blood of pregnant women has been rapidly adopted as a screening test for the detection of disorders involving chromosomal aneuploidy, especially Down syndrome. However as part of a prenatal recommendation in high-risk group, this laboratory assessment should be accompanied by informed counseling at both pre-test and post-test stages. In low-risk group and multifetal pregnancies, only conventional maternal serum screening tests in the first trimester and/or second trimester in addition to measurement of nuchal translucency should be recommended, until this potential tool has been incorporated into current screening strategic modalities on the basis ofsufficient published data." @default.
• W2024456811 created "2016-06-24" @default.
• W2024456811 creator A5001591774 @default.
• W2024456811 date "2014-01-01" @default.
• W2024456811 modified "2023-10-07" @default.
• W2024456811 title "Clinical application of non-invasive prenatal testing using cell free fetal DNA" @default.
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• W2024456811 doi "https://doi.org/10.5124/jkma.2014.57.9.771" @default.
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