Ignite Creation Date:
2024-05-05 @ 9:42 AM
Last Modification Date:
2024-10-26 @ 9:04 AM
Study NCT ID:
NCT00004351
Status:
COMPLETED
Last Update Posted:
2005-06-24
First Post:
1999-10-18
Brief Title:
Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
Sponsor:
National Institute of Neurological Disorders and Stroke NINDS
Organization:
Office of Rare Diseases ORD
Conditions & Keywords Data
Conditions:
| Name |
|---|
| Williams Syndrome |
| Angelman Syndrome |
| Prader-Willi Syndrome |
| Shprintzen Syndrome |
| Smith-Magenis Syndrome |
| DiGeorge Syndrome |
| Chromosome Abnormalities |