Cite
HARVARD Citation
Ryan, A. et al. (2017). Comment on "Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods". Prenatal diagnosis. pp. 725-726. [Online].
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Ryan, A. et al. (2017). Comment on "Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods". Prenatal diagnosis. pp. 725-726. [Online].