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Molecular Genetics Of Heterotaxy And Related Congenital Heart Defects

Study Overview

The purpose of this study is to obtain information from individuals and their families with heterotaxy and related congenital heart defects in order to elucidate the molecular genetics of this disorder.

Study Description

The goal of this study is to obtain specimens and data from individuals and their families with heterotaxy and related congenital heart defects in order to clarify the molecular genetics of this disorder.

Additional Information

Participants may be compensated for their participation.


  • IRB Number: 1403871897
  • Research Study Identifier: TX6875
  • Principal Investigator: Stephanie Ware, MD

Recruitment Status

Open

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Contact Us

If you need help finding a study or have any questions, please contact us at inhealth@iu.edu or by phone at (888) 264-0005.