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The Journal of Clinical Psychiatry|November 4, 2015
Impact of psychiatric comorbidity and cognitive deficit on function in 22q11.2 deletion syndromeJames J Yi, Monica E Calkins, Sunny X Tang, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|August 25, 2014
Subthreshold psychotic symptoms in 22q11.2 deletion syndromeSunny X Tang, James J Yi, Tyler M Moore, et al.
Biological Psychiatry|January 4, 2015
Aberrant Cortical Morphometry in the 22q11.2 Deletion SyndromeJ Eric Schmitt, Simon Vandekar, James Yi, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Molecular Cytogenetics|May 13, 2008
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplicationBlake C Ballif, Aaron Theisen, Justine Coppinger, et al.
The Laryngoscope|September 21, 2024
Hearing Loss in Children with 22q11.2 Deletion SyndromeJill Arganbright, Terrence Blaine Crowley, Meghan Tracy, et al.
American Journal of Human Genetics|January 10, 2002
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisShih-hsin Kan, Navaratnam Elanko, David Johnson, et al.
Journal of Medical Genetics|February 24, 2011
Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotypeM Balasubramanian, K Smith, L Basel-Vanagaite, et al.
American Journal of Human Genetics|October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone developmentM A Simpson, R Hsu, L S Keir, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 18, 2018
Autosomal dominant mannose-binding lectin deficiency is associated with worse neurodevelopmental outcomes after cardiac surgery in infantsDaniel Seung Kim, Yatong K Li, Jerry H Kim, et al.
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