Clinical trial
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
NCT00004351
Drugs and interventions used in this trial
0 registeredThese interventions are listed by ClinicalTrials.gov. An RxNorm link indicates a mapped medicine record; the registry name alone is not proof of a specific branded formulation.
No interventions are currently published for this study in CureCurrent. View the original registry record below.
Study at a glance
Registry-backedStudy of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
Design: OBSERVATIONAL · Status: COMPLETED · Phase: Not specified
Read study objectives, eligibility and outcome measures at ClinicalTrials.govAdvertisement
Conditions
Williams Syndromeverified · MONDO: Williams syndrome
Angelman Syndromeverified · MONDO: Angelman syndrome
Shprintzen Syndromeunresolved
DiGeorge Syndromeverified · MONDO: DiGeorge syndrome
Chromosome Abnormalitiesunresolved
Interventions
Sponsors & collaborators
Baylor College of Medicinecollaborator
Mapped research locations
Registry source
Open the source record to verify current eligibility, contacts, locations and registry updates.
Open NCT00004351 on ClinicalTrials.gov ↗Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.