Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory’s Retrospecti... by Erica Soster, Brittany Dyr, Samantha Caldwell, Amanda Sussman, Hany Magharyous

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Positive cfDNA screening results for 22q11.2 deletion syndrome—Clinical and laboratory considerations by Erica Soster, Brittany Dyr, Jill Rafalko, Jill Rafalko, Eyad Almasri, Phillip Cacheris

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Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray by Erica Soster, John Tynan, Clare Gibbons, Wendy Meschino, Jenna Wardrop, Eyad Almasri, Stuart Schwartz, Graham McLennan

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Application of mosaicism ratio to multifetal gestations. by Jill Rafalko, Samantha Caldwell, Erica Soster, Eyad Almasri, Graham McLennan, Tong Liu, Vivian Weinblatt, Philip Cacheris, Ron McCullough

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Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium by Erica Soster, Tamara Mossfield, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois, Jean Gekas, Tristan Hardy, Kelly Loggenberg, on behalf of the Global Expanded NIPT Consortium

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Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes by Tamara Mossfield, Erica Soster, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois, Jean Gekas, Tristan Hardy, Monika Jurkowska, Pascale Kleinfinger, Kelly Loggenberg, Pablo Marchili, Roberto Sirica, on behalf of the Global Expanded NIPT Consortium

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