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

Clinical trial NCT00004351 · COMPLETED

Trial details

NCT number: NCT00004351
Sponsor: National Institute of Neurological Disorders and Stroke (NINDS)
Status: COMPLETED
Study type: OBSERVATIONAL

Williams Syndrome Angelman Syndrome Prader-Willi Syndrome Shprintzen Syndrome Smith-Magenis Syndrome DiGeorge Syndrome Chromosome Abnormalities

Start date: 1999-09-01
Enrollment: 20

View on ClinicalTrials.gov

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