Contribution of High-throughput Exome Sequencing in the Diagnosis of the Cause Fetal Polymalformation Syndromes

Clinical trial NCT02512354 · COMPLETED

Trial details

NCT number: NCT02512354
Sponsor: Centre Hospitalier Universitaire Dijon
Status: COMPLETED
Study type: OBSERVATIONAL

Fetuses With at Least 2 Malformations, and no Diagnosis After Fetopathological and Radiological Examinations

Start date: 2015-03-04
Primary completion: 2018-10-08
Enrollment: 100

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