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==Overview==
==Overview==


'''22q11.2 deletion syndrome''' is a disorder caused by the deletion of a small piece of [[chromosome 22 (human)|chromosome 22]]. The deletion occurs near the middle of the [[chromosome]] at a location designated q11.2. It has a prevalence estimated at 1:4000.<ref name="pmid14736631">{{cite journal |author=Oskarsdóttir S, Vujic M, Fasth A |title=Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden |journal=Arch. Dis. Child. |volume=89 |issue=2 |pages=148-51 |year=2004 |pmid=14736631 |doi=}}</ref>
'''22q11.2 deletion syndrome''' is a disorder caused by the deletion of a small piece of [[chromosome 22 (human)|chromosome 22]]. The deletion occurs near the middle of the [[chromosome]] at a location designated q11.2.


==References==
==References==

Revision as of 14:47, 4 September 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

22q11.2 deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.

References

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