Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreatedTANG, S. X; YI, J. J; GUR, R. E et al.Psychological medicine (Print). 2014, Vol 44, Num 6, pp 1267-1277, issn 0033-2917, 11 p.Article

Speech and Hearing in Adults with 22q11.2 Deletion SyndromePERSSON, Christina; FRIMAN, Vanda; OSKARSDOTTIR, Solveig et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 12, pp 3071-3079, issn 1552-4825, 9 p.Article

Eye Gaze During Face Processing in Children and Adolescents With 22q11.2 Deletion SyndromeGLASER, Bronwyn; DEBBANE, Martin; OTTET, Marie-Christine et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2010, Vol 49, Num 7, pp 665-674, issn 0890-8567, 10 p.Article

Clinically detectable copy number variations in a Canadian catchment population of schizophreniaBASSETT, Anne S; COSTAIN, Gregory; WAILUNALANFUNG et al.Journal of psychiatric research. 2010, Vol 44, Num 15, pp 1005-1009, issn 0022-3956, 5 p.Article

Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcomeSCHNEIDER, Maude; VAN DER LINDEN, Martial; MENGHETTI, Sarah et al.Journal of psychiatric research. 2014, Vol 48, Num 1, pp 86-93, issn 0022-3956, 8 p.Article

Growth Charts for 22q11 Deletion SyndromeTARQUINIO, Daniel C; JONES, Marilyn C; LYONS JONES, Kenneth et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2672-2681, issn 1552-4825, 10 p.Article

Velopharyngeal Dysfunction and 22q11.2 Deletion Syndrome: A Longitudinal Study of Functional Outcome and Preoperative Prognostic FactorsSPRUIJT, N. E; WIDDERSHOVEN, J. C. C; BREUGEM, C. C et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 4, pp 447-455, issn 1055-6656, 9 p.Article

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphismsSHASHI, Vandana; FRANCIS, Alan; HOOPER, Stephen R et al.European journal of human genetics. 2012, Vol 20, Num 10, pp 1051-1057, issn 1018-4813, 7 p.Article

Occurrence of affective disorders compared to other psychiatric disorders in children and adolescents with 22q11.2 deletion syndromeJOLIN, Edith M; WELLER, Ronald A; WELLER, Elizabeth B et al.Journal of affective disorders. 2012, Vol 136, Num 3, pp 222-228, issn 0165-0327, 7 p.Article

Mapping Cortical Morphology in Youth With Velocardiofacial (22q 11.2 Deletion) SyndromeKATES, Wendy R; BANSAL, Ravi; FREMONT, Wanda et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2011, Vol 50, Num 3, pp 272-282, issn 0890-8567, 11 p.Article

Velopharyngeal anatomy in 22q11.2 deletion syndrome : A three-dimensional cephalometric analysisRUOTOLO, Rachel A; VEITIA, Nestor A; ARENS, Raanan et al.The Cleft palate-craniofacial journal. 2006, Vol 43, Num 4, pp 446-456, issn 1055-6656, 11 p.Article

Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: A comparison of prodromal psychotic symptoms and general functioningARMANDO, Marco; GIRARDI, Paolo; SCHÄFER, Miriam R et al.Schizophrenia research. 2012, Vol 139, Num 1-3, pp 151-156, issn 0920-9964, 6 p.Article

Cognitive phenotype of velocardiofacial syndrome: A reviewFURNISS, Frederick; BISWAS, Asit B; GUMBER, Rohit et al.Research in developmental disabilities (Print). 2011, Vol 32, Num 6, pp 2206-2213, issn 0891-4222, 8 p.Article

Memory in intellectually matched groups of young participants with 22q11.2 deletion syndrome and those with schizophreniaKRAVARITI, Eugenia; JACOBSON, Clare; MORRIS, Robin et al.Research in developmental disabilities (Print). 2010, Vol 31, Num 3, pp 864-868, issn 0891-4222, 5 p.Article

Chromosome 22q11.2 Deletion Syndrome in African-American Patients: A Diagnostic ChallengeVEERAPANDIYAN, Aravindhan; ABDUL-RAHMAN, Omar A; SHASHI, Vandana et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2186-2195, issn 1552-4825, 10 p.Article

Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndromeSTODDARD, Joel; NIENDAM, Tara; HENDREN, Robert et al.Schizophrenia research. 2010, Vol 118, Num 1-3, pp 118-121, issn 0920-9964, 4 p.Article

Antibody Deficiency in Adults With 22q11.2 Deletion SyndromeBJÖRK, Aron H; OSKARSDOTTIR, Sólveig; ANDERSSON, Bengt A et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 1934-1940, issn 1552-4825, 7 p.Article

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndromeMACHADO, Alexei M. C; SIMON, Tony J; NGUYEN, Vy et al.Brain research. 2007, Vol 1131, pp 197-210, issn 0006-8993, 14 p.Article

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?ANGKUSTSIRI, Kathleen; GOODLIN-JONES, Beth; DEPREY, Lesley et al.Journal of autism and developmental disorders. 2014, Vol 44, Num 4, pp 739-746, issn 0162-3257, 8 p.Article

A Case of Congenitally Absent Left Internal Carotid Artery: Vascular Malformations in 22q11.2 Deletion SyndromeJOHNSON, Matthew D; GENTRY, Lindell R; RICE, Gregory M et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 3, pp 314-317, issn 1055-6656, 4 p.Article

Unrelated Chromosomal Anomalies Found in Patients With Suspected 22qll.2 DeletionFEMANDEZ, Luis; LAPUNZINA, Pablo; GALAN-GOMEZ, Enrique et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 9, pp 1134-1141, issn 1552-4825, 8 p.Article

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 Deletion Syndrome)KATES, Wendy R; MILLER, Adam M; ABDULSABUR, Nuria et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2006, Vol 45, Num 5, pp 587-595, issn 0890-8567, 9 p.Article

Computerized Neurocognitive Profile in Young People With 22q11.2 Deletion Syndrome Compared to Youths With Schizophrenia and At-Risk for PsychosisGOLDENBERG, Paula C; CALKINS, Monica E; CONROY, Catherine G et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2012, Vol 159, Num 1, pp 87-93, issn 1552-4841, 7 p.Article

Extracardiac features predicting 22qll.2 Deletion Syndrome in adult congenital heart diseaseFUNG, Wai Lun Alan; CHOW, Eva W. C; WEBB, Gary D et al.International journal of cardiology. 2008, Vol 131, Num 1, pp 51-58, issn 0167-5273, 8 p.Article

Possible mechanisms and gene involvement in speech problems in the 22q11.2 deletion syndromeWIDDERSHOVEN, J. C. C; BEEMER, F. A; KON, M et al.Journal of plastic, reconstructive & aesthetic surgery. 2008, Vol 61, Num 9, pp 1016-1023, issn 1748-6815, 8 p.Article