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RECRUITING
NCT03065686
NA

Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing

Sponsor: Centre Hospitalier Universitaire, Amiens

View on ClinicalTrials.gov

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

Interventions

GENETIC

identification of genetic factors

Clinical questionnaire and analysis of genetic data obtained by exome high-throughput sequencing

Locations (1)

CHU Amiens Picardie

Amiens, France