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2 studies found for:    17467974 [PUBMED-IDS]
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Rank Status Study
1 Recruiting Development of the Tool " iPSC " for the Functional Study of Mutations Responsible for Mental Retardation
Conditions: Intellectual Deficiency;   Asymptomatic Carrier of the Mutation of the Gene MYT1L;   Healthy Volunteers
Intervention: Procedure: Cutaneous biopsy
2 Completed Microarray Analysis in Syndromic Obesity
Conditions: Mental Retardation;   Syndromic Obesity
Intervention: Genetic: Clinical examination and blood sampling for biological and genetic analysis

Study has passed its completion date and status has not been verified in more than two years.