In prenatal diagnostics, chromosomal microarray analysis (CMA) improved the diagnostic rate for chromosomal abnormalities by 4.1–10% compared with traditional karyotyping in fetuses with ultrasound ...
Single nucleotide polymorphisms (SNPs) are one of the most common determinants and potential biomarkers of human disease pathogenesis. SNPs could alter amino acid residues, leading to the loss of ...
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