Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.

Por Wang, T, Okano, Y, Eisensmith, R, Huang, S Z, Zeng, Y T, Lo, W H, Woo, S L
Publicado em 1989

IgD multiple myeloma with thoracic spine compression due to epidural extra-osseous tumour spread.

Por Lolin, Y I, Lam, C W, Lo, W H, Au, K L, Masarei, J R
Publicado em 1994

Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in Asia.

Por Wang, T, Okano, Y, Eisensmith, R C, Lo, W H, Huang, S Z, Zeng, Y T, Woo, S L
Publicado em 1991

Founder effect of a prevalent phenylketonuria mutation in the Oriental population.

Por Wang, T, Okano, Y, Eisensmith, R C, Harvey, M L, Lo, W H, Huang, S Z, Zeng, Y T, Yuan, L F, Furuyama, J I, Oura, T
Publicado em 1991

Polymorphic microsatellites and Wilson disease (WD)

Por Stewart, E. A., White, A., Tomfohrde, J., Osborne-Lawrence, S., Prestridge, L., Bonne-Tamir, B., Scheinberg, I. H., George-Hyslop, P. St, Giagheddu, M., Kim, J.-W., Seo, J. K., Lo, W. H.-y., Ivanova-Smolenskaya, I. A., Limborska, S. A., Cavalli-Sforza, L. L., Farrer, L. A., Bowcock, A. M.
Publicado em 1993