Genetics and Psychopathology in the 22q11 Deletion Syndrome
NCT00161109 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 175
Last updated 2006-10-13
Summary
The purposes of this study are to:
1. study the nature and longitudinal course of psychiatric symptoms in children with the 22q11.2 deletion syndrome and
2. identify genes that contribute to the occurrence of these symptoms.
Conditions
- Chromosome 22q11.2 Deletion Syndrome
Sponsors & Collaborators
-
Netherlands Brain Foundation
collaborator OTHER -
Children's Hospital of Philadelphia
collaborator OTHER -
UMC Utrecht
lead OTHER
Principal Investigators
-
René S. Kahn, M.D., Ph.D. · UMC Utrecht, The Netherlands
Eligibility
- Min Age
- 8 Years
- Max Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2002-10-31
- Completion
- 2012-10-31
Countries
- United States
- Netherlands
Study Locations
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