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1. Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay   
Kyung Yeon Lee, Eunsim Shin
Korean J Pediatr. 2017 September;60(9):282-289.  Publication Date (Online): 2017 September 15
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2. 1p36 deletion syndrome confirmed by fluorescence in situ hybridization and array-comparative genomic hybridization analysis   
Dong Soo Kang, Eunsim Shin, Jeesuk Yu
Korean J Pediatr. 2016 November;59(Suppl 1):S14-18.  Publication Date (Online): 2016 November 30
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3. 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, Jin-Hwa Moon, Se-Min Lee, Joo-Hwa Kim, Jae-Won Oh, Chang-Ryul Kim, In Joon Seol
Korean J Pediatr. 2016 February;59(2):91-95.  Publication Date (Online): 2016 February 15
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4. A case of isodicentric chromosome 15 presented with epilepsy and developmental delay   
Jon Soo Kim (Kim JS), Jinyu Park (Park JY), Byung-Joo Min (Min BJ), Sun Kyung Oh (Oh SK), Jin Sun Choi (Choi JS), Mi Jung Woo (Woo MJ), Jong Hee Chae (Chae JH), Ki Joong Kim (Kim KJ), Yong Seung Hwang (Hwang YS), Byung Chan Lim (Lim BC)
Korean J Pediatr. 2012 December;55(12):487-490.  Publication Date (Online): 2012 September 03
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