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

Contact the research team to learn more about this study.

Fields marked with asterisk (*) are required

Please verify that you are not a bot.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.

Volunteer Sign up

Volunteer Registry

Create your profile and be matched to research opportunities

Register Now!

If you need assistance finding a study or if you have any questions, please email: ctsirro@iu.edu or call us at (317) 278-2176