C. Lam

Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria.

S. Tam, Chi-kong Lai, Y. Yuen, 2006, Kidney international.

Heterogeneous mutations of the ATP2C1 gene causing Hailey–Hailey disease in Hong Kong Chinese

T. Cheng, K. Ho, C. Lam, 2010, Journal of the European Academy of Dermatology and Venereology : JEADV.

Permanent Cardiac Pacemaker: an Emergency Perspective

C. Lam, 2001 .

Lathosterolosis: a disorder of cholesterol biosynthesis resembling smith-lemli-opitz syndrome.

S. Tam, V. Wong, C. Fung, 2014, JIMD reports.

Diagnostic Difficulties in Sanfilippo Disease

S. Lam, C. Lam, D. Chan, 2006 .

Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy

S. Tam, T. Siu, G. C. Chan, 2007, Journal of Inherited Metabolic Disease.

De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring

L. Wong, C. Lam, P. W. Tse, 2001, Journal of paediatrics and child health.

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

V. Wong, S. Tam, C. Fung, 2010, Molecular genetics and metabolism.

Genetic Testing and Personalized Medicine

C. Lam, 2010 .