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American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
Neurocase|March 25, 2005
Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptomsCarrie E Bearden, Theo G M van Erp, John R Monterosso, et al.
Genes|January 21, 2023
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective StudyHayley A Ron, Terrence Blaine Crowley, Yichuan Liu, et al.
Human Molecular Genetics|December 19, 2003
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletionSulagna C Saitta, Stacy E Harris, Ann P Gaeth, et al.
Biological Psychiatry|November 12, 2016
The Psychosis Spectrum in 22q11.2 Deletion Syndrome Is Comparable to That of Nondeleted YouthsSunny X Tang, Tyler M Moore, Monica E Calkins, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 23, 2013
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndromeJames J Yi, Sunny X Tang, Donna M McDonald-McGinn, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 23, 2005
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion SyndromeCarrie E Bearden, Abbas F Jawad, David R Lynch, et al.
The American Journal of Psychiatry|September 1, 2004
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndromeCarrie E Bearden, Abbas F Jawad, David R Lynch, et al.
Neuroimage. Clinical|September 14, 2016
Disrupted anatomic networks in the 22q11.2 deletion syndromeJ Eric Schmitt, James Yi, Monica E Calkins, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 5, 2008
Proline affects brain function in 22q11DS children with the low activity COMT 158 alleleJacob A S Vorstman, Bruce I Turetsky, Monique E J Sijmens-Morcus, et al.
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