P067: Identification of novel variant in WT1 gene in African-American girl with Denys-Drash syndrome by Jasmine Lee, Meghan McGath, Berrin Monteleone

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P382: Presentation of dual molecular diagnoses of two patients with neurodevelopmental disorder by Defne Ercelen, Berrin Monteleone, Meghan McGath

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P614: Prenatal diagnosis of anopthalmia with de novo variant in SOX2 by Jennifer Kidd, Emily Schneider, Berrin Monteleone, Meghan McGath, Martin Chavez

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P632: Absent ductus venosus as a prenatal ultrasound finding of Noonan syndrome by Emily Schneider, Jennifer Kidd, Meghan McGath, Berrin Monteleone, Patricia Rekawek, Martin Chavez

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Estimating health state utilities for aromatic L-amino acid decarboxylase deficiency (AADCd) in the United States by Berrin Monteleone, Katie Forster, Gin Nie Chua, Rongrong Zhang, Andrew Lloyd, Paul Castellano, Ioannis Tomazos

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Patient selection considerations for AADC deficiency gene therapy by Agathe Roubertie, Irina Anselm, Bruria Ben‐Zeev, Wuh‐Liang Hwu, Ashutosh Kumar, Berrin Monteleone, Shin‐ichi Muramatsu, Vincenzo Leuzzi, Salvador Ibáñez, Scellig Stone, Phillip L. Pearl

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