Fetal RhD NIPT: do all Rh negative patients need Rh immune globulin?
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Panorama
Resources related to Panorama non-invasive prenatal testing (NIPT).
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The evolution of NIPT: what comes next
In this talk, we will highlight how early, highly accurate prenatal screening optimizes outcomes for patients with 22q11.2 deletion syndrome, and review recently-published data from a large clinical v
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Clinical Validation of a SNP-based Prenatal Cell-free DNA Screening Test for Fetal RHD Status in a Large US Cohort
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Fetal RhD NIPT: A new testing option to inform care for RhD alloimmunized patients and those at risk
Natera™'s Fetal RhD NIPT (noninvasive prenatal testing) is now available. The test is backed by the largest clinical validation study for fetal RhD in the US to date, and demonstrated 100 percent sens
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Clinical Validation of a SNP-based Prenatal Cell-free DNA Screening Test for Fetal RHD Status in a Large US Cohort
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It's time to screen routinely for 22q11.2 deletion syndrome: new evidence of improved outcomes with prenatal diagnosis
To manage pregnancies at high risk for 22q11.2 deletion syndrome (DS), prenatal and neonatal evaluation after high risk cfDNA screening is needed. Supplemental assessments and early intervention can i
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Compassionate Care Application - Spanish
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Carrier Manifestations in Pregnancy
Utility of carrier screening to inform management
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Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from t
Martin et al. 2023 Prenat. Diagn
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Natera Product Brochure
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Validation of an Enhanced Version of a Single- Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies
Ryan A, Hunkapiller N, Banjevic M, et al. Fetal Diagn Ther 2016
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Informatics-based, highly accurate, noninvasive prenatal paternity testing
Ryan A, Baner J, Demko Z, et al. Genet Med 2013
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Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphismebased noninvasive prenatal test
Curnow KJ, Wilkins-Haug L, Ryan A, et al. Am J Obstet Gynecol 2015
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Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fe
Norwitz ER, McNeill G, Kalyan A, et al. Journal of Clinical Medicine 2019
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Re: Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate
Jelsema R, Demko ZP, Billing, PR. Ultrasound Obstet Gynecol. 2020
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Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing
Schmidt JL, Pizzino A, Nicholl J et al. American Journal of Medical Genetics Part A
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Primary cell-free DNA screening or contingent screening for the common trisomies: a response
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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Introduction to Genetic Counseling Roles in Industry
Genetic Counselor Awareness Day 2023
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NSGC Annual Conference Flyer 2023
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