P638: Identification of a pathogenic variant in NSDHL in a patient with congenital high airway obstruction (CHAOS) syndrome by Asha Talati, Edward Spence, Neeta Vora, William Goodnight

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P809: Diagnosis and management of pregnant people with inborn errors of metabolism in an adult reproductive genetics and genomics clinic by Asha Talati, Emily Hardisty, Madeline Dyke, Clara Hildebrandt, Michael Adams, Muge Calikoglu, Neeta Vora

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P320: Novel variant in DSP associated with lethal acantholytic epidermolysis bullosa and bradyarrhythmia by Asha Talati, Joseph Cornett, Brianna Frame, Emily Hardisty, Sarah White, Neeta Vora, Elizabeth Jalazo

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P813: Experiences of Black pregnant people offered prenatal diagnosis in the setting of fetal anomalies: A qualitative study by Asha Talati, Karen Sheffield-Abdullah, Aryana Daye, Kelly Gilmore, Marsha Michie, Anne Lyerly, Neeta Vora

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P637: Single center experience using single-gene-NIPT to evaluate fetal risk of autosomal recessive conditions by Asha Talati, Emily Hardisty, Kelly Gilmore, Rachel Veazey, Ginger Hocutt, Smriti Singh, Madeline Dyke, Neeta Vora

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P799: Experiences with an adult reproductive clinical genetics and genomics clinic: Insights and opportunities by Madeline Dyke, Asha Talati, Emily Hardisty, Smriti Singh, Kelly Gilmore, Rachel Veazey, Ginger Hocutt, Amy Mottola, Neeta Vora

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O44: Diagnostic yield of amniocentesis in pregnancies ≥24 weeks: An international multicenter study* by Roni Zemet Lazar, Mohamad Ali Maktabi, Alexandra Tinfow, Jessica Giordano, Thomas Heisler, Qi Yan, Roni Plaschkes, Michal Berkenstadt, Boaz Weisz, David Crosby, Jennifer Walsh, Siobhán Corcoran, Juliana Gebb, Erica Schindewolf, Kendra Miller, Kate Swanson, Teresa Sparks, Asha Talati, Neeta Vora, Ronald Wapner, Ignatia Van Den Veyver

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