earticle

Lee, Woong-Woo, Choi, Jong-Moon, Lee, Cha Gon

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.17 No.1 2020 pp.34-38

Smith-Kingsmore syndrome: The first report of a Korean patient with the MTOR germline mutation c.5395G>A p.(Glu1799Lys)

Lee, Dohwan, Jang, Ja-Hyun, Lee, Cha Gon

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.16 No.1 2019 pp.27-30

Jang, Min Jeong, Lee, Cha Gon, Kim, Hyun Jung

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.15 No.2 2018 pp.110-114

A family with X-linked Cornelia de Lange syndrome due to a novel SMC1A missense mutation identified by multi-gene panel sequencing

Hong, Sungwon, Lee, Cha Gon

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.15 No.1 2018 pp.24-27

Xeroderma pigmentosum group A with mutational hot spot (c.390-1G>C in XPA ) in South Korea

Choi, Jung Yoon, Yun, Hyung Ho, Lee, Cha Gon

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.13 No.1 2016 pp.20-25

Clinical outcome of acute necrotizing encephalopathy in related to involving the brain stem of single institution in Korea

Lee, Cha Gon, Kim, Ji Hye, Lee, Munhyang, Lee, Jeehun

[Kisti 연계] 대한소아과학회 Korean journal of pediatrics Vol.57 No.6 2014 pp.264-270

Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH

Lee, Cha Gon, Yun, Jun-No, Park, Sang-Jin, Sohn, Young Bae

[Kisti 연계] 대한의학유전학회 Journal of genetic medicine Vol.10 No.1 2013 pp.52-56

심한 폐동맥 고혈압을 동반한 좌우 단락 질환 환자의 수술 후 경과

이차곤, 정수인, 허준, 강이석, 이흥재, 양지혁, 전태국

[Kisti 연계] 대한소아과학회 Korean journal of pediatrics Vol.53 No.2 2010 pp.195-202

초극소 미숙아에서 발생한 중증 태아 수종을 동반한 폐혈관 공기 색전증 1례

김묘징, 유희준, 이차곤, 박수경, 장윤실, 박원순

[Kisti 연계] 대한소아과학회 Korean journal of pediatrics Vol.52 No.12 2009 pp.1392-1395