Cite
HARVARD Citation
LaHaye, S. et al. (2016). Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circulation. p. . [Online].
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LaHaye, S. et al. (2016). Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circulation. p. . [Online].