DOI: 10.1055/s-00000089

Ultraschall in der Medizin - European Journal of Ultrasound

References

Gross SJ, Stosic M, McDonald-McGinn DM. et al.
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11. 2 deletion syndrome.

Ultrasound Obstet Gynecol 2016;
47: 177-183

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