Clinical Trials Logo

16P12.2 Microdeletion clinical trials

View clinical trials related to 16P12.2 Microdeletion.

Filter by:
  • None
  • Page 1

NCT ID: NCT01238250 Recruiting - ASXL1 Gene Mutation Clinical Trials

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

Start date: October 2010
Phase:
Study type: Observational

Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have gene changes that are linked to autism and other neurodevelopmental disorders. 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.