L. Law

Expanded newborn metabolic screening programme in Hong Kong: a three-year journey.

Y. Yuen, J. Hui, S. Chong, 2017, Hong Kong medical journal = Xianggang yi xue za zhi.

Inherited metabolic diseases in the Southern Chinese population; Diseases Spectrum and estimated incidence from recurrent mutations

Josephine S. C. Chong, N. Tang, T. Fok, 2016 .

Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations.

Josephine S. C. Chong, Chi-kong Li, T. Fok, 2014, Pathology.

A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients

W. Hwu, L. Law, N. Tang, 2002, Human mutation.

Classical galactosaemia in Chinese: A case report and review of disease incidence

T. Fok, N. Tang, L. Law, 1999, Journal of paediatrics and child health.

Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families

T. Fok, A. Chan, N. Tang, 2000, Human mutation.

Case Report: 3-Methyglutaconic Aciduria in a Chinese Patient with Glycogen Storage Disease Ib

T. Fok, J. Hui, C. Lam, 2003, Journal of Inherited Metabolic Disease.