Viewing Study NCT00004351

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Ignite Creation Date: 2025-12-24 @ 11:39 PM
Ignite Modification Date: 2026-04-10 @ 12:36 AM
Study NCT ID: NCT00004351
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-10-18
Is NOT Gene Therapy: True
Has Adverse Events: False
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:
Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Williams Syndrome View
None Angelman Syndrome View
None Prader-Willi Syndrome View
None Shprintzen Syndrome View
None Smith-Magenis Syndrome View
None DiGeorge Syndrome View
None Chromosome Abnormalities View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Angelman syndrome View
None DiGeorge syndrome View
None Prader-Willi syndrome View
None Shprintzen syndrome View
None Smith-Magenis syndrome View
None Williams syndrome View
None genetic diseases and dysmorphic syndromes View
None neurologic and psychiatric disorders View
None rare disease View