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Showing results 1 to 4 of 4

Issue Date	Title / Author(s) / Citation	File
2002	Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome Chae, Jong Hee; Hwang, Yong Seung; Kim, Ki Joong J Child Neurol 2002;17:33-36	link
2005-05	Mutational analysis of idiopathic renal hypouricemia in Korea Cheong, Hae Il; Kang, Ju Hyung; Lee, Joo Hoon; Ha, Il Soo; Kim, Suhnggwon; Komoda, Fusako; Sekine, Takashi; Igarashi, Takashi; Choi, Yong Pediatr Nephrol. 2005 Jul;20(7):886-90. Epub 2005 May 24.	link
2006-02	Two cases of isolated diffuse mesangial sclerosis with WT1 mutations Hahn, Hyewon; Cho, Young Mi; Park, Young Seo; You, Han Wook; Cheong, Hae Il J Korean Med Sci. 2006 Feb;21(1):160-4.	view file link
2007-11	Identification of a novel DHCR7 mutation in a Korean patient with Smith-Lemli-Opitz syndrome Chae, Jong Hee; Kim, Ki Joong; Hwang, Yong Seung; Ki, Chang-Seok; Kim, Jong-Won J Child Neurol. 2007 Nov;22(11):1297-300.	link