Talk:Chromosome 22q11.2 deletion syndrome

From Citizendium
Revision as of 18:21, 24 November 2009 by imported>Daniel Mietchen (started)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
This article is a stub and thus not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
To learn how to update the categories for this article, see here. To update categories, edit the metadata template.
 Definition A genetic disorder due to deletions in human chromosome 22, preferentially affecting the development of the cardiovascular, neural and immune systems. [d] [e]
Checklist and Archives
 Workgroup categories Health Sciences and Biology [Categories OK]
 Talk Archive none  English language variant British English