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Accuracy of fetal fraction measurements in a single nucleotide polymorphismbased noninvasive prenatal test

Accuracy of fetal fraction measurements in a single nucleotide polymorphismbased noninvasive prenatal test

Published Date February 26, 2025

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Fetal RhD NIPT Patient Video - Arabic
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The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model

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about 2 months ago
Duran family's 22q story

The Duran family shares their 22q story, and the importance of early detection and diagnosis.

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2 months ago
22q11.2 Deletion Syndrome (DiGeorge): Two cases, two outcomes. The importance of prenatal identification

22q11.2 deletion syndrome, also known as DiGeorge, is caused by a missing section of chromosome 22. It is more common than other conditions routinely screened for prenatally such as cystic fibrosis, s

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3 months ago
Fetal RhD NIPT Patient Video - Vietnamese

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3 months ago
Fetal RhD NIPT Patient Video - Spanish

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3 months ago
Fetal RhD NIPT Patient Video - Russian

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3 months ago
Fetal RhD NIPT Patient Video - Chinese

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3 months ago
Fetal RhD NIPT Patient Video - Arabic

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4 months ago
The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model

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5 months ago
Fetal RhD NIPT: Transforming care for Rh negative pregnant patients

Until recently, there has not been a reason to diverge from the standard approach of giving Rh immune globulin to all Rh negative patients. That has changed with the introduction of fetal RhD NIPT, no

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6 months ago
Fetal RhD NIPT Patient Video

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7 months ago
Clinical Validation of a Prenatal Cell-Free DNA Screening Test for Fetal RHD in a Large U.S. Cohort

Gilstrop Thompson, et al. OBSTETRICS & GYNECOLOGY 2024

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7 months ago
22q11.2 Deletion Syndrome (DiGeorge): Its impact on families and why early detection matters

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7 months ago
Genetic Counselor Awareness Day 2024

Introduction to Genetic Counseling Roles in Industry

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8 months ago
Importance of high detection 22q screening

Dr. Sam Leonard, Sr. Medical Director (Natera), walks through how to appropriately consider the balance between high detection rates and screen positive rates when selecting a screen.

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8 months ago
Importance of 22q screening and KOL testimonial

Dr. Blagowidow, OB Geneticist, talks about the importance of early prenatal 22q11.2 deletion syndrome (22q, formerly DiGeorge syndrome) screening and factors to consider when selecting a screen.

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9 months ago
Fetal RhD NIPT: do all Rh negative patients need Rh immune globulin?

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11 months ago
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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about 1 year ago
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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about 1 year ago
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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about 1 year ago
Clinical Validation of a SNP-based Prenatal Cell-free DNA Screening Test for Fetal RHD Status in a Large US Cohort

Read More

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The tests described have been developed and their performance characteristics determined by the CLIA-certified laboratory performing the test. The tests have not been cleared or approved by the US Food and Drug Administration (FDA). CAP accredited, ISO 13485 certified, and CLIA certified. © 2024 Natera, Inc. All Rights Reserved.