Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening–detectable findings
Idit Maya, Liat Salzer Sheelo, Dana Brabbing‐Goldstein, Reut Matar, Sarit Kahana, Ifaat Agmon‐Fishman, Cochava Klein, Merav Gurevitch, Lina Basel‐Salmon, Lena Sagi‐Dain
Topics & Concepts
MedicinePrenatal screeningCopy-number variationPrenatal diagnosisAmniocentesisObstetricsPregnancyMicroarrayResidual riskFetusBioinformaticsGeneticsInternal medicineGenomeBiologyGeneGene expressionPrenatal Screening and DiagnosticsGenomic variations and chromosomal abnormalitiesFetal and Pediatric Neurological Disorders