Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology
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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia
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Molecular Psychiatry, 2023, vol. 28, p.2071-2080
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
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