Case Report: An association of left ventricular outflow tract obstruction with 5p deletions von Mascho, Kira, Yatsenko, Svetlana A, Lo, Cecilia W, Xu, Xinxiu, Johnson, Jennifer, Helvaty, Lindsey R, Burns Wechsler, Stephanie, Murali, Chaya N, Lalani, Seema R, Garg, Vidu, Hodge, Jennelle C, McBride, Kim L, Ware, Stephanie M, Lin, Jiuann-Huey Ivy

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A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease von Landis, Benjamin J, Helvaty, Lindsey R, Geddes, Gabrielle C, Lin, Jiuann-Huey Ivy, Yatsenko, Svetlana A, Lo, Cecilia W, Border, William L, Wechsler, Stephanie Burns, Murali, Chaya N, Azamian, Mahshid S, Lalani, Seema R, Hinton, Robert B, Garg, Vidu, McBride, Kim L, Hodge, Jennelle C, Ware, Stephanie M

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Performance of Dysmorphology‐Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing von Helm, Benjamin M., Helvaty, Lindsey R., Conboy, Erin, Geddes, Gabrielle C., Graham, Brett H., Lah, Melissa, Wetherill, Leah, Landis, Benjamin J., Ware, Stephanie M.

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A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices von Durbin, Matthew D., Helvaty, Lindsey R., Li, Ming, Border, William, Fitzgerald-Butt, Sara, Garg, Vidu, Geddes, Gabrielle C., Helm, Benjamin M., Lalani, Seema R., McBride, Kim L., McEntire, Alexis, Mitchell, Dana K., Murali, Chaya N., Wechsler, Stephanie B., Landis, Benjamin J., Ware, Stephanie M.

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Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery von Landis, Benjamin J, Helm, Benjamin M, Durbin, Matthew D, Helvaty, Lindsey R, Herrmann, Jeremy L, Johansen, Michael, Geddes, Gabrielle C, Ware, Stephanie M

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Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects von Durbin, Matthew D., Fairman, Korre, Helvaty, Lindsey R., Huang, Manyan, Li, Ming, Abreu, Daniel, Geddes, Gabrielle C., Helm, Benjamin M., Landis, Benjamin J., McEntire, Alexis, Mitchell, Dana K., Ware, Stephanie M.

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Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return von Huth, Emily A, Zhao, Xiaonan, Owen, Nichole, Luna, Pamela N, Vogel, Ida, Dorf, Inger L H, Joss, Shelagh, Clayton-Smith, Jill, Parker, Michael J, Louw, Jacoba J, Gewillig, Marc, Breckpot, Jeroen, Kraus, Alison, Sasaki, Erina, Kini, Usha, Burgess, Trent, Tan, Tiong Y, Armstrong, Ruth, Neas, Katherine, Ferrero, Giovanni B, Brusco, Alfredo, Kerstjens-Frederikse, Wihelmina S, Rankin, Julia, Helvaty, Lindsey R, Landis, Benjamin J, Geddes, Gabrielle C, McBride, Kim L, Ware, Stephanie M, Shaw, Chad A, Lalani, Seema R, Rosenfeld, Jill A, Scott, Daryl A

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Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return von Huth, Emily A, Zhao, Xiaonan, Owen, Nichole, Luna, Pamela N, Vogel, Ida, Dorf, Inger L.H, Joss, Shelagh, Clayton-Smith, Jill, Parker, Michael J, Louw, Jacoba J, Gewillig, Marc, Breckpot, Jeroen, Kraus, Alison, Sasaki, Erina, Kini, Usha, Burgess, Trent, Tan, Tiong Y, Armstrong, Ruth, Neas, Katherine, Ferrero, Giovanni B, Brusco, Alfredo, Kerstjens-Frederikse, Wihelmina S, Rankin, Julia, Helvaty, Lindsey R, Landis, Benjamin J, Geddes, Gabrielle C, McBride, Kim L, Ware, Stephanie M, Shaw, Chad A, Lalani, Seema R, Rosenfeld, Jill A, Scott, Daryl A

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