An inside look at Natera’s SMFM Lineup
Visit us at Booth #210
Connect with our team to learn how we’re advancing prenatal genetics and supporting MFMs through high-quality testing, streamlined workflows, and clinician-led education resources that strengthen care delivery.
Oral Presentations
Performance of a single gene non-invasive prenatal screening test for recessive conditions. Oral Plenary Session 1 | Wednesday February 11 8:45 AM
Development and Validation of a SNP-based cfDNA test for vanishing twin pregnancies: The VANISH Trial. Oral Concurrent Session 6 | Thursday February 12 1:00 PM
Lunch Symposium | Wednesday, February 11 | 12:00–1:00 pm | Academy 407–409
Beyond Aneuploidy: The Evolving Role of Single-Gene NIPT in Clinical Practice. Explore the evolution of NIPT and the expanding clinical insights available through innovations of cfDNA screening, including emerging applications for autosomal dominant, X-linked, and recessive conditions. Lunch will be provided. Hosted by Jeffrey Dungan, MD with speaker Michelle Owens MD, MS, FACOG.
Be sure to sign up when registering for the conference
Prenatal Genetics Lunch Meeting | Thursday, February 12 | 12:00–1:00 pm
This interactive forum brings together trainees and faculty for round-table discussions on key issues in prenatal genetics, including AR single-gene NIPT, prenatal sequencing, and VUS re-evaluation, with opportunities for mentorship and collaboration.
Be sure to sign up when registering for the conference
Poster Presentations
Carrier Screening as Pathway to In-Utero Therapy: Carrier Frequencies for Conditions with Prenatal Intervention Potential
Identification of maternal Alzheimer’s disease risk after an atypical finding on SNP-based prenatal cfDNA screening