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For contributors- 1p36 deletion syndrome confirmed by fluorescence
in situ hybridization and array-comparative genomic hybridization analysis - Dong Soo Kang, Eunsim Shin, Jeesuk Yu
- Clin Exp Pediatr. 2016;59(Suppl 1):S14-S18.
- Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay
- Kyung Yeon Lee, Eunsim Shin
- Clin Exp Pediatr. 2017;60(9):282-289.
- A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
- Young-Jin Choi, Eunsim Shin, Tae Sik Jo et al.
- Clin Exp Pediatr. 2016;59(2):91-95.