Prenatal molecular evaluation of six fetuses in four unrelated Korean families with ornithine transcarbamylase deficiency.

Por Yoo, H. W., Kim, G. H.
Publicado em 1998

Comparison of enzyme and DNA analysis in a Tay-Sachs disease carrier screening program.

Por Yoo, H. W., Astrin, K. H., Desnick, R. J.
Publicado em 1993

Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene.

Por Warner, C A, Yoo, H W, Roberts, A G, Desnick, R J
Publicado em 1992

Clinical correlations of peripheral blood microchimerism after liver transplantation.

Por Kim, K. M., Kim, E. J., Yoo, H. W., Seo, J. J., Lee, S. G.
Publicado em 2000

A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome

Por Clayton, P, Chatelain, P, Tatò, L, Yoo, H W, Ambler, G R, Belgorosky, A, Quinteiro, S, Deal, C, Stevens, A, Raelson, J, Croteau, P, Destenaves, B, Olivier, C
Publicado em 2013

Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndrome

Por Stevens, A, Clayton, P, Tatò, L, Yoo, H W, Rodriguez-Arnao, M D, Skorodok, J, Ambler, G R, Zignani, M, Zieschang, J, Della Corte, G, Destenaves, B, Champigneulle, A, Raelson, J, Chatelain, P
Publicado em 2014

Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trial

Por Kim, J., Suh, B.-K., Ko, C. W., Lee, K.-H., Shin, C. H., Hwang, J. S., Kim, H. S., Chung, W. Y., Kim, C. J., Han, H.-S., Kwon, N. Y., Cho, S. Y., Yoo, H.-W., Jin, D.-K.
Publicado no J Endocrinol Invest (2017)