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Fadl-Elmula I, Abdel-Raheem SY, Khalid R. Atypical case of Rett syndrome with concurrent MECP2 gene mutation and del(15)(q22qter) karyotype: A case report and review of literature. World J Clin Pediatr 2025; 14(4): 109874 [PMID: 41255665 DOI: 10.5409/wjcp.v14.i4.109874]
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