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For contributors- Clinical application of whole exome and genome sequencing in pediatric neurodevelopmental disorders
- Keun Soo Lee, Seung Hwan Oh, Ja Young Lee et al.
- Clin Exp Pediatr. 2026;69(5):417-427.
- Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
- Go Hun Seo, Ja Hye Kim, Ja Hyang Cho et al.
- Clin Exp Pediatr. 2016;59(1):16-23.