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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date
	Analysis of inborn errors of metabolism: Disease spectrum for expanded newborn screening in Hong Kong Journal:Chinese Medical Journal	Lee, HCH Mak, CM Lam, CW Yuen, YP Chen, AOK Shek, CC Siu, TS Lai, CK Ching, CK Siu, WK Chen, SPL Law, CY Tai, MHL Tam, S Chan, AYW	2011
	Application of pharmacogenetics: UGT1A128 and nilotinib-induced unconjugated hyperbilirubinaemia in a patient with chronic myeloid leukaemia Journal:Pathology*	Chen, SPL Poon, WT Mak, CM Lam, CW Kwong, YL Chan, AYW Tam, S	2011
	Effect of the microsomal triglyceride transfer protein -493 G/T polymorphism and type 2 diabetes mellitus on LDL subfractions Proceeding/Conference:Hong Kong Medical Journal	Chen, SPL Tan, KCB Lam, KSL	2003
	Effect of the microsomal triglyceride transfer protein -493 G/T polymorphism and type 2 diabetes mellitus on LDL subfractions Journal:Atherosclerosis	Chen, SPL Tan, KCB Lam, KSL	2003
	Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients Journal:Journal of Clinical Pathology	Mak, CM Siu, WK Law, CY Wong, CK Lee, HK Yeung, S Sham, CO Tse, K Lee, HHC Chen, SPL Ching, CK Au, CK Poon, WT Lam, CW Kwong, NS Chan, AYW	2012
	Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience Journal:Hong Kong Medical Journal	Mak, CM Chen, SPL Mok, NS Siu, WK Lee, HHC Ching, DCK Tsui, PT Fong, NC Yuen, YP Poon, DWT Law, CY Chong, YK Chan, YW Yung, TC Fan, KY Lam, CW	2018
	Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients Journal:Hong Kong Medical Journal	Mak, CM Chan, KY Yau, EKC Chen, SPL Siu, WK Law, CY Lam, CW Chan, AYW	2011
	Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population Journal:Hormone and Metabolic Research	Lee, CHP Cheung, CYY Chow, WS Woo, YC Yeung, CY Lang, BHH Fong, CHY Kwok, KHM Chen, SPL Mak, CM Tan, KCB Lam, KSL	2015
	Influences of the microsomal triglyceride transfer protein gene polymorphism on plasma lipids and lipoproteins in Southern Chinese Proceeding/Conference:International Huaxia Congress of Endocrinology, IHCE-2	Chen, SPL Tan, KCB Lam, KSL	2001
	NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome Journal:Clinica Chimica Acta	Lam, CW Law, CY Leung, KF Lai, CK Chen, SPL Chan, B Chan, KY Yuen, LYP Mak, CM Chan, AYW	2015
	Phenylketonuria in Hong Kong Chinese: A call for hyperphenylalaninemia newborn screening in the special administrative region, China Journal:Chinese Medical Journal	Mak, CM Ko, CH Lam, CW Lau, WL Siu, WK Chen, SPL Law, CY Lai, CK Yu, CM Chan, AYW	2011

Showing results 1 to 11 of 11