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European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|August 16, 2016
Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndromeRonnie Weinberger, James Yi, Monica Calkins, et al.
European Journal of Medical Genetics|August 16, 2017
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4Maria Francesca Bedeschi, Giuseppe Marangi, Maria Rosaria Calvello, et al.
Nature Reviews. Disease Primers|May 19, 2016
22q11.2 deletion syndromeDonna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, et al.
International Journal of Pediatric Otorhinolaryngology|June 25, 2014
22q11.2 Deletion syndrome and obstructive sleep apneaWilliam P Kennedy, Pamela A Mudd, Meg A Maguire, 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.
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.
Molecular Psychiatry|January 22, 2014
Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbiditiesR E Gur, J J Yi, D M McDonald-McGinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2016
Tracheal cartilaginous sleeves in children with syndromic craniosynostosisTara L Wenger, John Dahl, Elizabeth J Bhoj, et al.
American Journal of Medical Genetics|July 16, 1999
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletionM Gerdes, C Solot, P P Wang, et al.
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