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Results for “MYT1L”

3 trials

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Showing 3 of 3 results

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
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 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