G. Kim,

Molecular and Clinical Characterization of Korean Patients with Congenital Lipoid Adrenal Hyperplasia

H. Yoo, G. Kim, G. Kim,, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical phenotype and mutation spectrum of the CYP21A2 gene in patients with steroid 21-hydroxylase deficiency.

J. Ko, H. Yoo, H. Jin, 2012, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Evaluation for anti-inflammatory effects of Siegesbeckia glabrescens extract in vitro

Gun-Hee Kim, B. Kang, K. Hwang, 2011 .

Identification of new mutations in the ornithine transcarbamylase (OTC) gene in Korean families

H. Yoo, D-H Lee, G. Kim, 1996, Journal of Inherited Metabolic Disease.

Interleukin-18, transforming growth factor-β, and vascular endothelial growth factor gene polymorphisms and susceptibility to primary glomerulonephritis.

H. Seo, J.H. Cho, H. Ryu, 2010, Tissue antigens.

Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.

C. Ki, H. Yoo, S. Cho, 2013, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Identification of four novel mutations in five unrelated Korean families with Fabry disease

H. Yoo, M.-C. Lee, J-S Kim, 2000, Clinical genetics.

Analysis of PRSS1 and SPINK1 Mutations in Korean Patients With Idiopathic and Familial Pancreatitis

Kwi-Sook Choi, H. Yoo, Myung-Hwan Kim, 2009, Pancreas.