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Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing
Sponsor: Centre Hospitalier Universitaire, Amiens
Summary
Despite significant progress made in identification on numerous genes and gene pathways critical for craniofacial development, several approaches, ie mutation screening of specific candidates, association studies and even genome-wide scans have largely failed to reveal the molecular basis of NS human clefting
Official title: Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing GENEPIC
Key Details
Gender
All
Age Range
Any - Any
Study Type
INTERVENTIONAL
Enrollment
30
Start Date
2016-11-30
Completion Date
2027-11-30
Last Updated
2026-05-13
Healthy Volunteers
No
Conditions
Interventions
identification of genetic factors
Clinical questionnaire and analysis of genetic data obtained by exome high-throughput sequencing
Locations (1)
CHU Amiens Picardie
Amiens, France