Original ResearchObstetricsResidual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening–detectable findings
Obstetrics
Key words
chromosomal aberrations
chromosomal microarray
copy number variants
noninvasive prenatal screening
prenatal diagnosis
prenatal screening
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The authors report no conflict of interest.
No financial support was received for this work.
Cite this article as: Maya I, Sheelo LS, Brabbing-Goldstein D, et al. Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening–detectable findings. Am J Obstet Gynecol 2022;226:562.e1-8.
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