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ObjectiveTo assess the clinical implication of chromosomal microarray analysis (CMA) in prenatal diagnosis of MCDK.
MethodsThirty‐seven cases with MCDKs detected by prenatal ultrasound were enrolled in the study; 33 cases were isolated MCDKs and four cases were non‐isolated MCDKs. CMA was performed on the Affymetrix CytoScan HD platform. The frequencies of the detected CNVs were compared with 461...
Objective
To determine the type and frequency of pathogenic chromosomal abnormalities in fetuses diagnosed with congenital heart disease (CHD) using chromosomal microarray analysis (CMA) and validate next‐generation sequencing as an alternative diagnostic method.
Method
Chromosomal aneuploidies and submicroscopic copy number variations (CNVs) were identified in amniocytes DNA samples from CHD fetuses...
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