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For contributors- A compound heterozygous mutation in the
FMO3 gene: the first pediatric case causes fish odor syndrome in Korea - Ji Hyun Kim, Sung Min Cho, Jong-Hee Chae
- Clin Exp Pediatr. 2017;60(3):94-97.
- Hemophagocytic lymphohistiocytosis diagnosed by brain biopsy
- Hee Young Ju, Che Ry Hong, Sung Jin Kim et al.
- Clin Exp Pediatr. 2015;58(9):358-361.
- A case of Becker muscular dystrophy with early manifestation of cardiomyopathy
- Ki Hyun Doo, Hye Won Ryu, Seung Soo Kim et al.
- Clin Exp Pediatr. 2012;55(9):350-353.
- A case of isodicentric chromosome 15 presented with epilepsy and developmental delay
- Jon Soo Kim, Jinyu Park, Byung-Joo Min et al.
- Clin Exp Pediatr. 2012;55(12):487-490.