Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes. (1/16)

Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome. (2/16)

A patient with 22q11.2 deletion syndrome: case report. (3/16)

Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome. (4/16)

Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome. (5/16)

Proton magnetic resonance spectroscopy in 22q11 deletion syndrome. (6/16)

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. (7/16)

Delayed-onset hypoparathyroidism in an adolescent with chromosome 22Q11 deletion syndrome. (8/16)

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