22q11.2 deletion syndrome
Why to screen for 22q11.2 deletion syndrome during your pregnancy with NIPT.
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Why to screen for 22q11.2 deletion syndrome during your pregnancy with NIPT.
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A guide to discussing a result with low fetal fraction from Panorama NIPT with patients.
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Why it’s important to screen for microdeletion syndromes during your pregnancy with NIPT.
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A guide to discussing atypical findings from Panorama NIPT with patients
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In this presentation, we will review the importance of screening sooner for SCTs, therapies and interventions available to families where an SCT is identified, and read out performance data from SMART
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During this webinar series, Natera’s medical leadership team will review publications with significant findings from SNP-based NIPT results.
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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: Experience from clinic
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Replaced "About the Panorama Prenatal Screen"
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