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MFM Clinical Conundrum - Implications for 22q NIPT Screening for the MFM-Fetal Medicine Specialist

MFM Clinical Conundrum - Implications for 22q NIPT Screening for the MFM-Fetal Medicine Specialist

Published Date November 10, 2015

Previous Video

Screening for Microdeletions through NIPT - Dr. Ronald J. Wapner

Dr. Wapner presents results of the Panorama™ validation study, which evaluated the performance of non-invasive prenatal testing (NIPT)for five microdeletion syndromes via a single-nucleotide polymorph
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Panorama® Your Questions Answered

Most Recent Videos

2 months ago
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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3 months ago
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10 months ago
22q11.2 deletion syndrome

Why to screen for 22q11.2 deletion syndrome during your pregnancy with NIPT.

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10 months ago
Low fetal fraction results for clinicians

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10 months ago
Microdeletion syndromes

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12 months ago
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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about 1 year ago
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about 1 year ago
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This webinar will focus on our recent publication in Prenatal Diagnosis — Positive predictive value of a single nucleotide polymorphism (SNP)‐based NIPT for aneuploidy in twins.

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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.