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Clinical trial

Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes

NCT00004351 is registered in ClinicalTrials.gov with National Institute of Neurological Disorders and Stroke (NINDS) as lead sponsor.

NCT NCT00004351
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Registry record

As filed in ClinicalTrials.gov.

Title
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
Lead sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Phase
Observational
Overall status
Completed
Start date
September 30, 1999
Completion date
Not reported
Enrollment
20
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

angelman syndrome, chromosome abnormalities, digeorge syndrome, prader-willi syndrome, shprintzen syndrome, smith-magenis syndrome, williams syndrome