Clinical Research Directory

Browse clinical research sites, groups, and studies.

1 clinical study listed.

Healthy volunteers

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17Q11.2 Microduplication Syndrome (Disorder)

Tundra lists 1 17Q11.2 Microduplication Syndrome (Disorder) clinical trial. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT01238250

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

Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.

Gender: All

Updated: 2025-06-06

2 states

16P11.2 Deletion Syndrome

16p11.2 Duplications

1Q21.1 Deletion

+181