Full Text View
Tabular View
No Study Results Posted
Related Studies
Genetic Modifiers for 22q11.2 Syndrome (VCFS)
The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2010 by State University of New York - Upstate Medical University.
Recruitment status was  Recruiting
Study NCT00916955   Information provided by State University of New York - Upstate Medical University

First Received on March 24, 2008.   Last Updated on August 4, 2010   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
22q11.2 Deletion Syndrome
Additional conditions recognized in this trial
DiGeorge Syndrome
More general conditions related to this trial
22q11 Deletion Syndrome
Abnormalities, Multiple
Cardiovascular Abnormalities
Cardiovascular Diseases
Chromosome Disorders
Congenital Abnormalities
Craniofacial Abnormalities
Endocrine System Diseases
Genetic Diseases, Inborn
Heart Defects, Congenital
Heart Diseases
Hypoparathyroidism
Lymphatic Abnormalities
Lymphatic Diseases
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Parathyroid Diseases
Interventions listed in this trial
Observation
Sponsors listed in this trial
State University of New York - Upstate Medical University
Albert Einstein College of Medicine of Yeshiva University


Contact Help Desk
Lister Hill National Center for Biomedical Communications,  U.S. National Library of Medicine,
U.S. National Institutes of Health,  U.S. Department of Health & Human Services,
USA.gov,  Copyright,  Privacy,  Accessibility,  Freedom of Information Act

U.S. National Institutes of Health U.S. National Library of Medicine U.S. Department of Health & Human Services