Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease - Concepedia

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Publication | Open Access

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease

DOI Full Paper Access

81

Citations

100

References

2016

Year

Stephanie LaHaye, Don Corsmeier, Madhumita Basu, Jessica Bowman, Sara Fitzgerald‐Butt, Gloria Zender, Kevin Bosse, Kim L. McBride, Peter White, Vidu Garg

Circulation Cardiovascular Genetics

Abstract

URL: https://clinicaltrials.gov; Unique Identifier: NCT0112048.

References

	Year	Citations

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