L. Chan

A frequent activated smoothened mutation in sporadic basal cell carcinomas

F. McCormick, Jingwu Xie, H. Ng, 1999, Oncogene.

Apolipoprotein E promoter and α2-Macroglobulin polymorphisms are not genetically associated with Chinese late onset Alzheimer's disease

M. Bullido, I. Sastre, C. Pang, 1999, Neuroscience Letters.

Genotype‐phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemia

B. Tomlinson, C. Pang, L. Baum, 2002, Human mutation.

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

V. Wong, C. Pang, T. Fok, 2000, Journal of medical genetics.

patients with infantile autism and Rett syndrome gene in MECP2 Spectrum of mutations in the

V. Wong, C. Pang, C. Lam, 2006 .

Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes

B. Tomlinson, C. Pang, L. Baum, 2003, Human mutation.

Apolipoprotein E genotype and its pathological correlation in Chinese Alzheimer's disease with late onset.

C. Pang, L. Baum, H. Ng, 1999, Human pathology.

[Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes].

C. Pang, M. Tsang, C. Lam, 2003, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.