Abstract
More than fifty percent of normal 46, XX results of early miscarriage samples analyzed by traditional karyotype, are due to maternal cell contamination (Lathi et al. 2014). This error is eliminated by SNP microarrays with Parental Support™ (Natera). We sought to review the incidence, type, and origin of chromosomal abnormalities detected by SNP microarray technology in patients who experienced first trimester miscarriage.
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