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

por Yoo, H. W., Kim, G. H.
Publicado 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 1993

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 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 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 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 2017