22q11.2 deletion syndrome overview: Difference between revisions
Jump to navigation
Jump to search
(Created page with "__NOTOC__ {{22q11.2 deletion syndrome}} {{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} ==Overview== '''22q11.2 deletion syndrome''' is a disorder caused by the deletion o...") |
|||
| Line 6: | Line 6: | ||
==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. | '''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
|
22q11.2 deletion syndrome Microchapters |
|
Differentiating 22q11.2 deletion syndrome from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
22q11.2 deletion syndrome overview On the Web |
|
American Roentgen Ray Society Images of 22q11.2 deletion syndrome overview |
|
Risk calculators and risk factors for 22q11.2 deletion syndrome overview |
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.