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Article

De novo variant of SETD1A causes neurodevelopmental disorder with dysmorphic facies: A case report.

Psychiatry and clinical neurosciences - 1 Feb 2022

Zhang Jia, Tao Qiuji, Yang Zuozhen, Li Yang, Gan Jing

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PMID: 34716975
DOI: 10.1111/pcn.13310
PMCID: PMC9300109

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De novo variant of SETD1A causes neurodevelopmental disorder with dysmorphic facies: A case report.PMID 34716975Read ↗

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[Schinzel-Giedion syndrome: a new mutation in SETBP1].Semantic proximity Read ↗

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Phenotypical and Genotypical Expansion of Autosomal-Dominant KDM1A -Related Neurodevelopmental Disorder Spectrum: A Case Report.Semantic proximity Read ↗

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