S-Space

Browse

Subject

Showing results 1 to 7 of 7

Issue Date	Title / Author(s) / Citation	File
2002	Mutation and aberrant expression of Caveolin-1 in human oral squamous cell carcinomas and oral cancer cell lines 한송이	link
2009-09	RUNX2 mutations in cleidocranial dysplasia patients. Ryoo, H-M; Kang, H-Y; Lee, S-K; Lee, K-E; Kim, J-W Oral Diseases 16:55-60	DOI
2009-10	Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta Choung, P.-H; Hyun, H.-K; Lee, S.-K; Lee, K.-E; Kang, H.-Y; Kim, E.-J; Kim, J.-W International Endontic Journal 42, 1039-1043	DOI
2010-01	RUNX2 mutations in cleidocranial dysplasia patients Ryoo, H-M; Kang, H-Y; Lee, S-K; Lee, K-E; Kim, J-W Oral Diseases (2010) 16, 55–60
2011-02	Runx2 돌연변이의 유전자형과 쇄골두개이형성증의 표현형의 인과관계 김태연	link
2016-08	A novel de novo mutation in LAMB3 causes localized hypoplastic enamel in the molar region Kim, Young-Jae; Shin, Teo J.; Hyun, Hong-Keun; Lee, Sang-Hoon; Lee, Zang H.; Kim, Jung-Wook EUROPEAN JOURNAL OF ORAL SCIENCES Vol.124 No.4, pp. 403-405	DOI
2016-08	A novel de novo mutation in LAMB3 causes localized hypoplastic enamel in the molar region Kim, Young-Jae; Shin, Teo J.; Hyun, Hong-Keun; Lee, Sang-Hoon; Lee, Zang H.; Kim, Jung-Wook European Journal of Oral Sciences, Vol.124 No.4, pp.403-405	DOI