Chromosome 22q11.2 deletion syndrome/Definition: Difference between revisions

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https://en.citizendium.org/wiki/index.php?title=Chromosome_22q11.2_deletion_syndrome/Definition&printable=yes
A definition or brief description of Chromosome 22q11.2 deletion syndrome.

A genetic disorder due to deletions in human chromosome 22, preferentially affecting the development of the cardiovascular, neural and immune systems.

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