Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
Shashi, V.; Keshavan, M. S.; Howard, T. D.; Berry, M. N.; Basehore, M. J.; Lewandowski, E.; Kwapil, T. R.; Clinical Genetics, 2006, vol. 69, issue 3, p 234, ISSN 00099163. ISBN 00099163.

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