1. Application of risk score analysis to low‐coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13. (23rd December 2015) Authors: Tynan, J. A.; Kim, S. K.; Mazloom, A. R.; Zhao, C.; McLennan, G.; Tim, R.; Liu, L.; Hannum, G.; Hull, A.; Bombard, A. T.; Oeth, P.; Burcham, T.; van den Boom, D.; Ehrich, M. Journal: Prenatal diagnosis Issue: Volume 36:Number 1(2016) Page Start: 56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗