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ObjectivesTo assess the frequency of karyotype abnormalities and chromosome 22q11.2 deletion syndrome among fetuses with abnormal cardiac ultrasound findings, and to evaluate the clinical value of chromosomal microarray‐based analysis (CMA) in the study of such pregnancies.
MethodsFirst, we carried out retrospective analysis of karyotype abnormalities and 22q11.2 deletion syndrome cases diagnosed...
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