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Author/Creator Oeth, P.

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) ↗

2. Circulating cell‐free fetal DNA for the detection of RHD status and sex using reflex fetal identifiers1. (6th December 2012)

Authors:
Moise, K. J.; Boring, N. H.; O'Shaughnessy, R.; Simpson, L. L.; Wolfe, H. M.; Baxter, J. K.; Polzin, W.; Eddleman, K. A.; Hassan, S. S.; Skupski, D.; McLennan, G.; Paladino, T.; Oeth, P.; Bombard, A.
Journal:
Prenatal diagnosis
Issue:
Volume 33:Number 1(2013:Jan.)
Page Start:
95
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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