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Clinical features of SMARCA2 duplication overlap with Coffin–Siris syndrome
Mar 2, 2025
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by
coffinsiris-foundation
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SMARCE1, a rare cause of Coffin–Siris Syndrome: Clinical description of three additional cases
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The role of objective facial analysis using FDNA in making diagnoses following whole exome analysis. Report of two patients with mutations in the BAF complex genes
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