Chromosome 22q11.2 microdeletion syndrome.
Chromosome 22q11.2 microdeletion syndrome is the most common microdeletion syndrome in humans. It involves the loss of genetic material on the short arm of one of the chromosome 22 alleles. Until advanced testing was available, this syndrome was known by various names including DiGeorge syndrome and...
| Published in: | Neonatal Network Vol. 30; no. 5; pp. 304 - 312 |
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| Format: | pictorial Journal Article |
| Published: |
Springer Publishing Company, Inc.
Sep/Oct2011
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| Online Access: | View this record in EBSCOhost |