Cite
HARVARD Citation
Artieri, C. et al. (2017). Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods. Prenatal diagnosis. pp. 482-490. [Online].
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Artieri, C. et al. (2017). Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods. Prenatal diagnosis. pp. 482-490. [Online].