Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study

Clinical trial NCT02862808 · COMPLETED

Trial details

NCT number: NCT02862808
Sponsor: Centre Hospitalier Universitaire de Besancon
Status: COMPLETED
Study type: OBSERVATIONAL

Severe Intellectual Disability

Start date: 2019-03-15
Primary completion: 2019-12-03
Enrollment: 18

View on ClinicalTrials.gov

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