Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome	22q11.2 deletion syndrome, Abnormalities, Multiple, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, DiGeorge syndrome, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, Musculoskeletal Abnormalities, cardiovascular disorder, chromosomal disorder, congenital heart disease, endocrine system disorder, heart disorder, hereditary disease, hypoparathyroidism, lymphatic system disorder, musculoskeletal system disorder, parathyroid gland disorder	Recruiting	Not stated	2026-07-29		NCT00556530

15 results · Page 1 of 1

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Organizations	Linked trials
Albert Einstein College of Medicine	48
Bambino Gesù Children's Hospital IRCCS	2
Cardiff University	16
Center for Inherited Disease Research (CIDR)	1
Children's Hospital of Philadelphia	215
KU Leuven	110
Maastricht University	40
National Heart, Lung, and Blood Institute (NHLBI)	791
National Institute on Aging (NIA)	571
Tel Aviv University	30
The Coriell Institute	1
Universidad del Desarrollo	8
University of California, Los Angeles	355
University of Geneva, Switzerland	42
University of Toronto	140

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Albert Einstein College Of Medicine	New York	United States	2