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• 17:20, 4 July 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (fixed interactions)
• 12:57, 4 July 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Added CLTC1 pathways)
• 21:44, 2 July 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (2 added pathways for COMT)
• 20:54, 2 July 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Added legend and fixed interactions)
• 16:42, 30 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (DGCR8 mediated DRD2 upregulation added)
• 21:55, 27 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (added pathway)
• 19:56, 27 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Added downstream genes)
• 12:03, 27 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (GP1BB downstream added)
• 10:21, 27 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Adding of gene functional descriptions)
• 11:53, 26 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Ontology Term : 'neurological disorder pathway' added !)
• 11:50, 26 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 11:50, 26 June 2019 Homo sapiens:22q11.2 copy number variation syndrome‎ (Ontology Term : 'velocardiofacial syndrome' added !)
• 13:42, 25 April 2019 N Victoravr‎ (Initial user page) (top)
• 13:42, 25 April 2019 N Victoravr‎ (Initial user page) (top)

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