https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:52402 Wed 28 Feb 2024 15:53:13 AEDT ]]> Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:45604 Wed 02 Nov 2022 14:06:59 AEDT ]]> Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:54501 Tue 27 Feb 2024 15:17:31 AEDT ]]> Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:42245 Tue 21 Mar 2023 19:04:35 AEDT ]]> Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:33797 Tue 15 Jan 2019 15:29:29 AEDT ]]> Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 deletion syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:17582 Sat 24 Mar 2018 08:03:58 AEDT ]]> Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:24111 Sat 24 Mar 2018 07:11:41 AEDT ]]> Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:39019 Fri 22 Apr 2022 09:10:54 AEST ]]>