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Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome
The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2009 by National Heart, Lung, and Blood Institute (NHLBI).
Recruitment status was  Recruiting
Study NCT00556530   Information provided by National Heart, Lung, and Blood Institute (NHLBI)

First Received on November 8, 2007.   Last Updated on August 7, 2009   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
DiGeorge Syndrome
22q11.2 Deletion 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
Sponsors listed in this trial
National Heart, Lung, and Blood Institute (NHLBI)


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