Curnow KJ, Wilkins-Haug L, Ryan A et al. Detection of triploid, molar, and vanishing-twin pregnancies by a single-nucleotide polymorphism-based non-invasive prenatal test. Am J ObstetGynecol 2014;211:x.ex-x.ex.

Dar P, Curnow KJ, Gross SJ, et al. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive aneuploidy testing. Am J ObstetGynecol 2014;211:527.e1-17

Pergament et al. Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort. Lippincott Williams & Wilkins 2014.

T. Takoudes and B. Hamar.Performance of non-invasive prenatal test when fetal cell-free DNA is absent. Ultrasound ObstetGynecol 2014.

Wapner RJ, Babiarz JE, Levy B, et al. Expanding the scope of noninvasive prenatal test: detection of fetal microdeletion syndromes. Am J ObstetGynecol 2014;212:….

Zimmermann et al. Non-invasive prenatal aneuploidy testing at chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci. PrenatDiagn. 2012 December;32(13):1233-1241. doi:10.1002/pd.3993

If you don’t tell them,
who will?

Join us in empowering your patients with
the best options in genetic screening.

Become a Provider

Joining our provider network is very simple.
All you need to do is

SMS CLARIA to 56767
or email us at
or dial 1800 – 1037590

Our representative will get in touch with you within 24 hours to help you with the registration. You can then start prescribing the test right away and help your patients gain clarity about their genetic health.