Kin-Chong Lau

发表

DNA-based diagnosis of mucolipidosis type IIIA and mucopolysacchariodisis type VI in a Chinese family: a chance of 1 in 7.6 trillion.

Chi-kong Li, M. S. Yan, C. Lam, 2007, Clinica chimica acta; international journal of clinical chemistry.

Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment.

C. Lam, P. Chan, W. Poon, 2011, Clinica chimica acta; international journal of clinical chemistry.

Microarrays for personalized genomic medicine.

C. Lam, S. Tong, Kin-Chong Lau, 2010, Advances in clinical chemistry.

Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.

C. Lam, D. Goh, H. Ong, 2013, Clinica chimica acta; international journal of clinical chemistry.

Automated imaging of circulating fluorocytes for the diagnosis of erythropoietic protoporphyria: a pilot study for population screening

C. Lam, Kin-Chong Lau, 2008, Journal of medical screening.

DNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population.

T. Siu, S. Tam, C. Lam, 2009, Clinica chimica acta; international journal of clinical chemistry.

Molecular investigations of a novel iduronate-2-sulfatase mutant in a Chinese patient.

C. Lam, Kin-Chong Lau, 2008, Clinica chimica acta; international journal of clinical chemistry.

Circulating fluorocytes at the first attack of acute intermittent porphyria: a missing link in the pathogenesis.

M. Tsang, C. Lam, C. Mak, 2011, Clinica chimica acta; international journal of clinical chemistry.

A fast modified protocol for random-access ultra-high density whole-genome scan: a tool for personalized genomic medicine, positional mapping, and cytogenetic analysis.

C. Lam, C. Mak, T. Tsoi, 2009, Clinica chimica acta; international journal of clinical chemistry.

Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.

C. Lam, D. Goh, H. Ong, 2013, Clinica chimica acta; international journal of clinical chemistry.