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Understanding the Role ofTbx1as a Candidate Gene for 22q11.2 Deletion Syndrome

✍ Scribed by Gao, Shan; Li, Xiao; Amendt, Brad A.


Book ID
121007033
Publisher
Current Science Inc.
Year
2013
Tongue
English
Weight
545 KB
Volume
13
Category
Article
ISSN
1529-7322

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## Abstract There is an overwhelming evidence that children and adults with 22q11.2 deletion syndrome (22q11.2DS) have a characteristic behavioral phenotype. In particular, there is a growing body of evidence that indicates an unequivocal association between 22q11.2DS and schizophrenia, especially