Status:

COMPLETED

Genetic Modifiers for 22q11.2 Syndrome

Lead Sponsor:

State University of New York - Upstate Medical University

Collaborating Sponsors:

Albert Einstein College of Medicine

Conditions:

22q11.2 Deletion Syndrome

Eligibility:

All Genders

Brief Summary

The purpose of the project is the determination of how the deletion of DNA from chromosome 22 at the q11.2 band causes the phenotypes observed in velo-cardio-facial syndrome (VCFS). In other words, th...

Eligibility Criteria

Inclusion

  • FISH confirmed diagnosis of 22q11.2 deletion syndrome

Exclusion

  • none

Key Trial Info

Start Date :

March 1 2008

Trial Type :

OBSERVATIONAL

End Date :

February 1 2015

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00916955

Start Date

March 1 2008

End Date

February 1 2015

Last Update

October 20 2021

Active Locations (1)

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Page 1 of 1 (1 locations)

1

VCFS International Center

Syracuse, New York, United States, 13210

Genetic Modifiers for 22q11.2 Syndrome | DecenTrialz