Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

Perez E, Sullivan KE. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes). Curr Opin Pediatr. 2002 Dec; 14(6):678-83.

View in: PubMed

subject areas

Abnormalities, Multiple
Animals
Autoimmune Diseases
Child
Chromosome Deletion
Chromosomes, Human, Pair 22
DiGeorge Syndrome
Facial Bones
Heart Defects, Congenital
Humans
Hypocalcemia
Infant, Newborn
Mice
Phenotype
Syndrome

authors with profiles

Kathleen Sullivan, APRN, PMHCNS-BC

RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

For technical support please contact support