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

Who can join

All ages · All sexes · Healthy volunteers welcome

Inclusion Criteria:

* 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

Exclusion Criteria:

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

About the study

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.

Sponsor: Rutgers, The State University of New Jersey · Participants: 800 · Started: 2013-07

Contact the study team

• Jennifer G Mulle, MHS, PhD · Phone: (848) 445-9866

Official record on ClinicalTrials.gov — NCT02447861

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.