Cite
HARVARD Citation
Tynan, J. et al. (2016). Application of risk score analysis to low‐coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13. Prenatal diagnosis. pp. 56-62. [Online].
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Tynan, J. et al. (2016). Application of risk score analysis to low‐coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13. Prenatal diagnosis. pp. 56-62. [Online].