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

RecruitingNAAges any - anyAllCentre Hospitalier Universitaire, Amiens
NCT03065686 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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

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📋 Eligibility rules (as published)
Inclusion Criteria: * Subject with a NSCL/P or CL/P of unknown etiology, * national health care insurance holders Exclusion Criteria: * Subject with a CL/P of known etiology, * Subject with a NSCL/P and an IRF6 mutation
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What it tests

  • identification of genetic factors
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Where

1 site
CHU Amiens Picardie
Amiens, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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