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Mar 31, 2024 · Abstract. Chromosome 22q11.2 deletion is among the strongest known genetic risk factors for neuropsychiatric disorders, including autism and ...
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Jan 3, 2023 · Microdeletion of a 3Mbp region encompassing 45 protein-coding genes at chromosome 22q11.2 (22q11.2DS) predisposes to multiple neurodevelopmental ...
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Mar 19, 2024 · Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome ; Lisanne Vervoort ; Nicolas Dierckxsens ...
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Nov 14, 2019 · Our results indicate that the 22q11.2 deletion reduces BBB integrity, alters the immune privilege of the CNS vasculature, and increases the ...
Missing: 3Dhttps% 2Fwww. 2Fcontent% 2F10. 2F2020. 02.14. 949784v2.
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Jun 23, 2023 · 2 Deletion Syndrome (22qDel) is a genetic Copy Number Variant (CNV) that strongly increases risk for schizophrenia and other neurodevelopmental ...
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Nov 14, 2019 · The 22q11.2 deletion includes junctional and mitochondrial genes that could influence barrier function (Arinami, 2006;. Devaraju & Zakharenko, ...
Missing: 3Dhttps% 2Fwww. 2Fcontent% 2F10. 2F2020. 02.14. 949784v2.
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