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Paper Details

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
Circ Cardiovasc Genet
59
2016
Author NameAffiliation
Stephanie LaHayeFrom the Center for Cardiovascular Research, The Research Institute (S.L., and Biomedical Genomics Core and the Center for Microbial Pathogenesis, The Research Institute (D.C., Nationwide Children's Hospital, The Ohio State University
Sara M Fitzgerald-ButtFrom the Center for Cardiovascular Research, The Research Institute (S.L., and Biomedical Genomics Core and the Center for Microbial Pathogenesis, The Research Institute (D.C., Nationwide Children's Hospital, The Ohio State University
Peter WhiteFrom the Center for Cardiovascular Research, The Research Institute (S.L., and Biomedical Genomics Core and the Center for Microbial Pathogenesis, The Research Institute (D.C., Nationwide Children's Hospital, The Ohio State University
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