Related references
Note: Only part of the references are listed.Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation
Nathaniel H. Robin et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
ADHD symptoms in children with FXS
Kelly Sullivan et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome
Ovsanna T. Leyfer et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2006)
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome)
WR Kates et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2006)