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Effects of Comt Genotype on Behavioral Symptomatology in the 22q11.2 Deletion Syndrome

โœ Scribed by Bearden, Carrie; Jawad, Abbas; Lynch, David; Monterossso, John; Sokol, Set; McDonald-McGinn, Donna; Saitta, Sulagna; Harris, Stacy; Moss, Edward; Wang, Paul; Zackai, Elaine; Emanuel, Beverly; Simon, Tony


Book ID
120831743
Publisher
Taylor and Francis Group
Year
2005
Tongue
English
Weight
108 KB
Volume
11
Category
Article
ISSN
0929-7049

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Candidate genes and the behavioral pheno
โœ Sarah E. Prasad; Sarah Howley; Kieran C. Murphy ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 154 KB

## 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