Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study
CompletedOBSERVATIONAL
Enrollment
18
Participants
Timeline
Start Date
March 15, 2019
Primary Completion Date
December 3, 2019
Study Completion Date
December 3, 2019
Conditions
Severe Intellectual Disability
Trial Locations (1)
25000
CHU Besancon, Besançon
All Listed Sponsors
lead
Centre Hospitalier Universitaire de Besancon
OTHER
NCT02862808 - Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study | Biotech Hunter | Biotech Hunter