T. J. Chen

Severe lactic acidosis caused by a novel frame-shift mutation in mitochondrial-encoded cytochrome c oxidase subunit II.

A. Gropman, L. Wong, M. Lipson, 2001, American journal of medical genetics.

Molecular genetics of glycogen-storage disease type 1a in Chinese patients of Taiwan.

W. Hwu, L. Wong, P. Dai, 2001, Molecular genetics and metabolism.

Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome.

L. Bird, M. Muenke, L. Wong, 2001, American journal of medical genetics.