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Natera Webinar Series Part III: What’s SMART about screening for sex chromosome trisomies : early intervention matters

Natera Webinar Series Part III: What’s SMART about screening for sex chromosome trisomies : early intervention matters

Published Date October 15, 2026

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Atypical finding results for clinicians

A guide to discussing atypical findings from Panorama NIPT with patients
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Natera Webinar Series Part II: NIPT for 22q11.2 DS: Does evidence support routine screening?

During this webinar series, Natera’s medical leadership team will review publications with significant findings from SNP-based NIPT results.

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A short informational video about Panorama™, Horizon™, and Fetal Focus™.

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Cathy Burson MS, CGC

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Melissa Hicks

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Duran family's 22q story

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

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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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over 1 year ago
Fetal RhD NIPT Patient Video - Vietnamese

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Fetal RhD NIPT Patient Video - Spanish

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Fetal RhD NIPT Patient Video - Russian

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Fetal RhD NIPT Patient Video - Chinese

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Fetal RhD NIPT Patient Video - Arabic

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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. © 2026 Natera, Inc. All Rights Reserved.