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HARVARD Citation
Gross, S. et al. (2016). Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome. Ultrasound in obstetrics & gynecology. pp. 177-183. [Online].
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Gross, S. et al. (2016). Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome. Ultrasound in obstetrics & gynecology. pp. 177-183. [Online].