UnknownNCT04382573

Better Delineation of CDK13 Related Phenotype and Epigenetic Signature.

Studying CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome

Last synced from ClinicalTrials.gov May 6, 2026

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Key facts

Sponsor: University Hospital, Montpellier
Principal Investigator: David GENEVIEVE
Department of Medical Genetics
Intervention: Epigenetic signatures(genetic)
Enrollment: 100 enrolled
Eligibility: All sexes
Timeline: 2019 – 2020

Study locations (1)

UH Montpellier, Montpellier, France

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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