T. Chan

Hyperammonemia in a girl who inherited a likely pathogenic variant of the ornithine transcarbamylase gene from her asymptomatic father—A peculiar pattern of X‐linked recessive inheritance

C. Shek, S. Chen, J. Chow, 2022, Clinical case reports.

Validation of amplicon-based next generation sequencing panel for second-tier test in newborn screening for inborn errors of metabolism

C. Mak, K. Tsang, T. Chan, 2021, Journal of Laboratory Medicine.

Survey on common reference intervals for general chemistry analytes in Hong Kong.

C. Mak, S. P. Chen, Y. Lo, 2019, Hong Kong medical journal = Xianggang yi xue za zhi.

Case Report: The first familial hCG syndrome in a Chinese family

C. Shek, S. Chen, Y. Cheung, 2021, F1000Research.

Determination of cerebrospinal fluid adenosine deaminase activity cut-off for the diagnosis of tuberculous meningitis in Hong Kong

C. Mak, C. Ching, S. Chen, 2020, Journal of Clinical Pathology.

Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey

E. Yau, Y. Lam, K. Ng, 2024, International Journal of Neonatal Screening.