The 22Q11.2 Deletion Syndrome

Soroosh Mahboubi

Abstract


22q11.2 deletion syndrome ( velocardiofacial syndrome) is one of the most common genetic syndromes it caused by a micro deletion of chromosome 22 at the q11.2 locus with a prevalence estimated 1 in 4,000 live births The condition may actually be more common than is estimate.

Full Text: PDF HTML

Refbacks

  • There are currently no refbacks.


Creative Commons License
This work is licensed under a Creative Commons Attribution 3.0 License.