A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy X by Zachary Demko, Brittany Prigmore, Peter Benn

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Screening for 22q11.2 deletion syndrome by two non-invasive prenatal testing methodologies: A case with discordant results by Liang-Ming Lo, Chii-Shinn Shiau, Kuang-Chao Chen, S.W.S. Shaw, Peter Benn

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Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis. by Paolo Guanciali Franchi, Chiara Palka, Elisena Morizio, Giulia Sabbatinelli, Melissa Alfonsi, Donatella Fantasia, Giammaria Sitar, Peter Benn, Giuseppe Calabrese

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P681: Carrier screening with the ACMG 113: An early look and new insights by Vivienne Souter, Erin Armentti, Madeleine Armer-Cabral, Emily Becraft, Jennifer Saucier, Elizabeth Repass, Linyan Meng, Peter Benn, Yang Wang

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Non-invasive prenatal screening: A 20-year experience in Italy by Chiara Palka, Paolo Guanciali-Franchi, Elisena Morizio, Melissa Alfonsi, Marco Papponetti, Giulia Sabbatinelli, Giandomenico Palka, Giuseppe Calabrese, Peter Benn

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P651: Bleeding complications in pregnant carriers of factor IX and factor XI ascertained through carrier screening by Lisa Johnson, Sarah Keilman, Emily Becraft, Elizabeth Repass, Peter Benn, Brittany Prigmore, Yang Wang, Bridget Maloney, Kayla Ruiz, Melda Balcioglu, Vivienne Souter

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Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single‐center study by Bryan J. Gall, Trevor B. Smart, Robin Munch, Supraja Kolluri, Hamsa Tadepally, Karen Phaik Har Lim, Zachary P. Demko, Peter Benn, Vivienne Souter, Nina Sanapareddy, Dianne Keen‐Kim

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