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Clinical trial

WAGR Syndrome and Other 11p Contiguous Gene Deletions: Clinical Characterization and Correlation With Genotype

NCT00758108 is registered in ClinicalTrials.gov with Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
WAGR Syndrome and Other 11p Contiguous Gene Deletions: Clinical Characterization and Correlation With Genotype
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Phase
Observational
Overall status
Completed
Start date
September 11, 2008
Completion date
April 29, 2015
Enrollment
197 (actual)
Sites
1

Conditions

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

aniridia, mental retardation, urogenital abnormalities, wagr syndrome, wilm's tumor