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Results for “MYT1L”

3 trials

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Showing 3 of 3 results

Not applicableStudy completedNCT02980302
What this trial is testing

Development of the Tool " iPSC " for the Functional Study of Mutations Responsible for Mental Retardation

Who this might be right for
Intellectual DeficiencyAsymptomatic Carrier of the Mutation of the Gene MYT1LHealthy Volunteers
University Hospital, Grenoble 4
Not applicableLooking for participantsNCT01238250
What this trial is testing

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

Who this might be right for
16P11.2 Deletion Syndrome16p11.2 Duplications1Q21.1 Deletion+181 more
Simons Searchlight 100,000
Not applicableLooking for participantsNCT07008612
What this trial is testing

MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder

Who this might be right for
MYT1L Syndrome
University Hospital, Rouen 50