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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

โœ Scribed by Gothelf, Doron; Eliez, Stephan; Thompson, Tracy; Hinard, Christine; Penniman, Lauren; Feinstein, Carl; Kwon, Hower; Jin, Shuting; Jo, Booil; Antonarakis, Stylianos E


Book ID
109940714
Publisher
Nature Publishing Group
Year
2005
Tongue
English
Weight
118 KB
Volume
8
Category
Article
ISSN
1097-6256

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Genotype and cardiovascular phenotype co
โœ Tingwei Guo; Donna McDonald-McGinn; Anna Blonska; Alan Shanske; Anne S. Bassett; ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 611 KB

Haploinsufficiency of TBX1, encoding a Tbox transcription factor, is largely responsible for the physical malformations in velo-cardio-facial /DiGeorge /22q11.2 deletion syndrome (22q11DS) patients. Cardiovascular malformations in these patients are highly variable, raising the question as to whethe