UnknownNCT00161109
Genetics and Psychopathology in the 22q11 Deletion Syndrome
Studying 22q11.2 deletion syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- UMC Utrecht
- Principal Investigator
- René S. Kahn, M.D., Ph.D.UMC Utrecht, The Netherlands
- Enrollment
- 175 enrolled
- Eligibility
- 8-20 years · All sexes
- Timeline
- 2002 – 2012
Study locations (2)
- Children's Hospital of Philadelphia, Dpt of Genetics and Dpt of Child and Adolescent Psychiatry, Philadelphia, Pennsylvania, United States
- UMC Utrecht, Dpt of Child and Adolescent Psychiatry, Utrecht, Netherlands
Collaborators
Netherlands Brain Foundation · Children's Hospital of Philadelphia
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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