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Ninalia NIPT The prenatal trisomy screening test based on maternal blood sample

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Resources and useful documents

Regulatory context

Scientific papers

Lo YM, Tein MS, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet. 1998;62(4):768-75.

Norton ME, Brar H, Weiss J, et al. Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. Am J Obstet Gynecol. 2012 Aug;207(2):127.e1-8. doi: 10.1016/j.ajog.2012.05.021. Epub 2012 Jun 1. PubMed PMID: 22742782.

Bianchi DW, Platt LD, Goldberg JD, et al. MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group. Genome-wide fetal aneyploidy detection by maternal plasma DNA sequencing. Obstet Gynecol. 2012;119(5):890-901.

Patricia A. Taneja, Holly L. Snyder, Eileen de Feo, Kristina M. Kruglyak, Meredith Halks-Miller, Kirsten J. Curnow and Sucheta Bhatt

Non-invasive prenatal testing in the general obstetric population: clinical performance and counseling considerations in over 85000 cases†. Prenat Diagn. 2016 Mar; 36(3): 237–243.

†Data was previously presented as an oral presentation at the Fetal Medicine Foundation (FMF),14th World Congress in Fetal Medicine, Crete, Greece, June 21–25, 2015.

Scientific information

Practical documents

Information leaflet for Ninalia NIPT


Find your nearest testing centre As Ninalia NIPT requires a specific sample tube, don’t forget to make an appointment in advance with your local laboratory for specimen collection.

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