NCT00004351View on ClinicalTrials.gov

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

CompletedOBSERVATIONAL
Enrollment

20

Participants

Timeline

Start Date

September 30, 1999

Conditions
Williams SyndromeAngelman SyndromePrader-Willi SyndromeShprintzen SyndromeSmith-Magenis SyndromeDiGeorge SyndromeChromosome Abnormalities
Trial Locations (1)

77030

Baylor College of Medicine, Houston

All Listed Sponsors
collaborator

Baylor College of Medicine

OTHER

lead

National Institute of Neurological Disorders and Stroke (NINDS)

NIH

NCT00004351 - Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes | Biotech Hunter | Biotech Hunter