P760: Impact of prenatal genetic diagnosis on pregnancy termination: Experience from a single center* by Carly Smith, Anuja Sule, Dena Matalon

Get full text

P353: From hypoplasia to aplasia of the trigeminal nerve: A recurring feature in the diagnosis of Gomez-Lopez-Hernandez syndrome by Juan Ramos, Emily Dunn, Hisham Damoush, Dena Matalon

Get full text

P253: Evaluating the clinical diagnostic yield of fragile X and chromosome microarray testing for patients with autism and/or intellectual disability by S.Y. Cindy Yang, Emily Dunn, Elizabeth Spiteri, Dena Matalon

Get full text

P295: Expanding the prenatal phenotype of a rare syndrome due to variants in DPH1 by Emily Dunn, Carly Smith, Catrina Loucks, A. Micheil Innes, Dena Matalon

Get full text

O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions by Courtney Verscaj, Frances Velez-Bartolomei, Ethan Bodle, Katie Chan, Michael Lyons, Willa Thorson, Wen-Hann Tan, John Graham, Angela Peron, Fabiola Quintero-Rivera, Elaine Zackai, Mary Ann Thomas, Cathy Stevens, Margaret Adam, Lynne Bird, Marilyn Jones, Dena Matalon

Get full text