Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome

Ultrasound in Obstetrics and Gynecology

Gross S, Stosic M, Basset A, McDonald-McGinn D, Norvez A, Dhamankar R, Kirkizlar E, Zimmermann B, Wayham N, Babiarz J, Ryan A, Jinnet K, Demko Z, Benn P. Ultrasound Obstet. Gynecol. 2016 Feb;47(2):177-83.