Clinical Trials for 16P13.11 Microdeletion Syndrome (Disorder)

Find clinical trials for 16p13.11 microdeletion syndrome (disorder). Discover research opportunities and treatment options in your area.

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

NCT ID: NCT01238250

The Simons Searchlight study is an online research program aimed at understanding how certain rare genetic changes relate to neurodevelopmental disorders and autism. This study collects important i...

Recruiting

Type: observational Locations: Boston, Massachusetts, United States, New York, New York, United States +1 more

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