Clinical Trial Update: Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

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Summary

A Simons Searchlight online study recruiting people with autism features associated with specific genetic changes, including 16p11.2 and 1q21.1 anomalies.

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Diseases / indications

• 16p11 Deletion Syndrome
• 16p11 Duplication Syndrome
• 1q21 Deletion Syndrome
• 1q21 Microduplication Syndrome
• Autism Spectrum Disorder

Snippet

Sponsor: Simons Searchlight | Conditions: 16P11.2 Deletion Syndrome, 16p11.2 Duplications | Status: RECRUITING