Cite
HARVARD Citation
Pertile, M. et al. (2021). Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies. Clinical chemistry. pp. 1210-1219. [Online].
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Pertile, M. et al. (2021). Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies. Clinical chemistry. pp. 1210-1219. [Online].