Clinically significant maternal X chromosomal copy number variation detected by noninvasive prenatal test
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DOI: 10.1111/jog.14033
Abstract: Maternal copy number variation (CNV), especially at the X chromosome is an important cause of false positive noninvasive prenatal test (NIPT) results for sex chromosomal aneuploidy. In addition, some maternal CNV can cause significant anomalies… read more here.
Keywords: copy number; number variation; maternal chromosomal; prenatal test ... See more keywords