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...
| Publicado en: | Neonatal Network Vol. 30; no. 5; pp. 304 - 312 |
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| Autor principal: | |
| Formato: | pictorial Journal Article |
| Publicado: |
Springer Publishing Company, Inc.
Sep/Oct2011
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| Acceso en línea: | Ver este registro en EBSCOhost |