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• W3100656308 abstract "Abstract Interstitial 8p deletions were previously described, in literature and databases, in approximately 30 patients with neurodevelopmental disorders. We report on a novel patient with a 8p21.2p11.21 deletion presenting a clinical phenotype that includes severe intellectual disability, microcephaly, epilepsy, and autism, the latter having been rarely associated with this genetic defect." @default.
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• W3100656308 date "2020-11-12" @default.
• W3100656308 modified "2023-10-18" @default.
• W3100656308 title "Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review" @default.
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• W3100656308 doi "https://doi.org/10.1002/ccr3.3523" @default.
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