The 3q29 Deletion and 3q29 Duplication: Architecture of Behavioral Phenotypes

Recruiting now

Conditions studied: Microdeletion 3q29 Syndrome, Microduplication 3q29 Syndrome

In brief

The 3q29 deletion syndrome is caused by a deletion of a small part of human chromosome 3, and the duplication syndrome is caused by a duplication of this same small region. The purpose of this study is to understand the medical and behavioral consequences of these syndromes.

Key facts

Study ID

NCT02447861

Run by

Rutgers, The State University of New Jersey

People needed

800

Starts

2013-07-01

Expected to finish

2028-01-01

Last updated by the study team

2026-05-20

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Diagnosis of 3q29 deletion or 3q29 duplication
• Consent from parents or guardians or an adult with 3q29 deletion or 3q29 duplication that does not require a legal guardian or an adult who is the healthy sibling of an individual with 3q29 deletion or 3q29 duplication or a healthy age-matched control

You may not qualify if…

• Clinically significant medical disease that would prohibit participation in the study procedures

Where it is running

• Internet-Based — Piscataway, New Jersey, United States (enrolling)

Full record on ClinicalTrials.gov

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