| Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Lahaye, S. Corsmeier, D. Basu, M. Bowman, J. L. Fitzgerald-Butt, S. Zender, G. Bosse, K. McBride, K. L. White, P. Garg, V. 2016 Enter body here... List Date: 11/21/16 |
