P631: Genome screening of newborns: What can we find and what’s next?* by Jorune Balciuniene, Ruby Liu, Jonathan Carmichael, Mauro Longoni, Sucheta Bhatt, Madhuri Hegde

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P649: The clinical utility of genome sequencing in the molecular diagnosis of genes related to inborn errors of metabolism by Xiangwen Chen-Deutsch, Mary Colasanto, Cristina da Silva, Christin Collins, Madhuri Hegde

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P730: Genetic basis of dysferlinopathy: A comprehensive analysis of sequence and copy number variants from a large cohort of 686 patients by Babi Ramesh Reddy Nallamilli, Mary Colasanto, Sreyanth Chandra Parupalli, Ruby Liu, Lakshmanan Jagannathan, Arul Joseph Duraisamy, Vinish Ramachander, Supan Dhillon, Madhuri Hegde

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P678: Role of de novo variants in genetic disorders with new insights and clinical implications by Babi Ramesh Reddy Nallamilli, Mary Colasanto, Ruby Liu, Naga Guruju, Lakshmanan Jagannathan, Arul Joseph Duraisamy, Jorune Balciuniene, Xiangwen Chen-Deutsch, Rizwan Yousaf, Christin Collins, Lora Bean, Supan Dhillon, Cristina da Silva, Madhuri Hegde

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