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Author/Creator Wayham, N.

1. Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome. (5th January 2016)

Authors:
Gross, S. J.; Stosic, M.; McDonald‐McGinn, D. M.; Bassett, A. S.; Norvez, A.; Dhamankar, R.; Kobara, K.; Kirkizlar, E.; Zimmermann, B.; Wayham, N.; Babiarz, J. E.; Ryan, A.; Jinnett, K. N.; Demko, Z.; Benn, P.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 47:Number 2(2016)
Page Start:
177
Record Type:
Journal Article
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