Associated Papers
Evaluation of the etiology of epilepsy and/or developmental delay in children via next-generation sequencing: a single-center experience.
Kava H et al.
Frontiers in Pediatrics, 2025
First Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants.
Reshadmanesh A et al.
Archives of Iranian Medicine, 2024
39891458 (PubMed )
Supplement: aim-27-700-s001.xlsx › Sheet2
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