Nationwide Children's Hospital is now utilizing whole exome sequencing (WES), with the addition of more traditional genetic techniques such as chromosomal microarray or traditional linkage analysis, to identify genetic causes of familial and isolated CHD.
| Study Type: |
Observational |
| Estimated Enrollment: |
1000 participants |
| Observational Model: |
Family-Based |
| Time Perspective: |
Prospective |
| Official Title: |
Genetics Testing of Individuals and Families With Congenital Heart Disease |
| Actual Study Start Date: |
December 2009 |
| Estimated Primary Completion Date: |
December 2025 |
| Estimated Study Completion Date: |
December 2025 |
Contact
| Contact: Vidu Garg, MD |
614-355-5710 vidu.garg@nationwidechildrens.org |
| ClinicalTrials.gov Identifier: |
NCT01192048 |
For enrollment please visit www.clinicaltrials.gov.
