- Advancing orphan drug development for rare diseases
- Jung Min Ko
- Clin Exp Pediatr. 2024;67(7):356-357.
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- Kabuki syndrome: clinical and molecular characteristics
- Chong-Kun Cheon, Jung Min Ko
- Clin Exp Pediatr. 2015;58(9):317-324.
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- The strong association of left-side heart anomalies with Kabuki syndrome
- Ja Kyoung Yoon, Kyung Jin Ahn, Bo Sang Kwon et al.
- Clin Exp Pediatr. 2015;58(7):256-262.
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- The natural history and prognostic factors of Graves' disease in Korean children and adolescents
- Seung Min Song, Ji-Seok Youn, Jung Min Ko et al.
- Clin Exp Pediatr. 2010;53(4):585-591.
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- A case of Smith-Lemli-Opitz syndrome diagnosed by identification of mutations in the 7-dehydrocholesterol reductase (DHCR7) gene
- Mee Rim Park, Jung Min Ko, Chong-Keun Cheon et al.
- Clin Exp Pediatr. 2008;51(11):1236-1240.
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- Genotype and clinical features of Korean patients with methylmalonic aciduria and propionic aciduria
- Eun Hye Lee, Jung Min Ko, Jae-Min Kim et al.
- Clin Exp Pediatr. 2008;51(9):964-970.
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- Phenotype-genotype correlations and the efficacy of growth hormone
treatment in Korean children with Prader-Willi syndrome
- Keun Wook Bae, Jung Min Ko, Han-Wook Yoo
- Clin Exp Pediatr. 2008;51(3):315-322.
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