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For contributors- Phelan-McDermid syndrome presenting with developmental delays and facial dysmorphisms
- Yoon-Myung Kim, In-Hee Choi, Jun Suk Kim et al.
- Clin Exp Pediatr. 2016;59(Suppl 1):S25-S28.
- 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.
- A Case of Ring Chromosome 21 with Multiple Congenital Anomalies
- Jun-Hwa Lee, Eul-Ju Seo
- Clin Exp Pediatr. 2003;46(3):291-294.