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

Rutgers, The State University of New Jersey · NCT02447861

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Any age listed · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
800
US sites recruiting
1
Study start
July 2013
Record last updated
May 20, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Conditions: Microdeletion 3q29 Syndrome; Microduplication 3q29 Syndrome

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

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

Recruiting US locations

  • Internet-Based

    Piscataway, NJ 08854

    Site contact: Jennifer Mulle, MHS, PhD · (848) 445-9866 · jennifer.mulle@rutgers.edu

Study contacts (from the official record)

  • Jennifer G Mulle, MHS, PhD · (848) 445-9866 · jennifer.mulle@rutgers.edu
  • Teresa Irving · tmi21@cabm.rutgers.edu
All healthy volunteers studies in New Jersey →
The 3q29 Deletion and 3q29 Duplication: Architecture of Behavioral… (NCT02447861) | Bored Studies