P492: A missense and nonsense variant combination in COASY resulting in severe prenatal onset PCH12: Expanding the clinical and genetic spectrum by Lindsey Walker, Miao Sun, Linda Randolph

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P773: A novel truncating variant in PRDM16 causes severe familial cardiomyopathy with variable clinical presentations by Miao Sun, Lindsey Walker, Nick Shillingford, Ramzi Bawab, Chao Shen, Jianjun Chen

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P796: Vanishing copy number gains: causative chromosomal changes or unstable findings of unknown consequence? by Avinash Dharmadhikari, Dolores Estrine, Katherine Ma, Lindsey Walker, Rosa Moreno, Matthew Deardorff, Linda Randolph, Gordana Raca

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P338: Studying the role of the DIP2C gene in humans and zebrafish by Katelyn Beatty, Ajay Deepak Verma, Madison Moe, Stephanie Htun, Thomas Scerri, Alpa Sidhu, Jacob Ginter, Lindsey Walker, Matthew Deardorff, Jenny Do, Ingrid van de Laar, Melissa Pauly, Georgia Vasileiou, Angela Morgan, Anne Slavotinek

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