EP11.13: Prenatal arterial tortuosity syndrome: a de facto late diagnosis by Al‐Obaidly, S., Kamal, R., Al‐Musafri, F., Al‐Ibrahim, A., Al‐Belushi, M., Saleh, N., Al‐Mansouri, Z., Kalache, K., Khenyab, N.

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EP09.11: Prenatal cephalocentesis: revisit the outcome by Al‐Obaidly, S., Al‐Mansouri, Z., Al‐Ibrahim, A., Saleh, N., Al‐Belushi, M., Al‐Musafri, F., Kalache, K., Khenyab, N.

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Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features by Stolerman, Elliot S., Francisco, Elizabeth, Stallworth, Jennifer L., Jones, Julie R., Monaghan, Kristin G., Keller‐Ramey, Jennifer, Person, Richard, Wentzensen, Ingrid M., McWalter, Kirsty, Keren, Boris, Heron, Benedicte, Nava, Caroline, Heron, Delphine, Kim, Katherine, Burton, Barbara, Al‐Musafri, Fatima, O'Grady, Lauren, Sahai, Inderneel, Escobar, Luis F., Meuwissen, Marije, Reyniers, Edwin, Kooy, Frank, Lacassie, Yves, Gunay‐Aygun, Meral, Schatz, Krista Sondergaard, Hochstenbach, Ron, Zwijnenburg, Petra J.G., Waisfisz, Quinten, Slegtenhorst, Marjon, Mancini, Grazia M.S., Louie, Raymond J.

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