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	Title	Author(s)	Issue Date	Views
	Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis Journal:Hong Kong Medical Journal	Lee, HHC Poon, KH Lai, CK Au, KM Siu, TS Lai, JPS Mak, CM Yuen, LYP Lam, CW Chan, AYW	2014	78
	Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz Syndrome Journal:Journal Of Inherited Metabolic Disease	Ho, CCA Fung, CW Siu, TS Ma, OCK Lam, CW Tam, S Wong, VCN	2014	84
	Molecular diagnosis for a fatal case of very long-chain Acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screening Journal:Diagnostic Molecular Pathology	Siu, WK Mak, CM Siu, SLY Siu, TS Pang, CY Lam, CW Kwong, NS Chan, AYW	2012	81
	Neurocognitive evaluation and plasma clozapine concentrations in Chinese patients with treatment-refractory schizophrenia Proceeding/Conference:International Journal of Neuropsychopharmacology	Chen, RYL Siu, TS Tam, S Chen, EYH	2002	143
	Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study Journal:Clinica Chimica Acta	Lee, HCH Lai, CK Yau, KCE Siu, TS Mak, CM Yuen, YP Chan, KY Tam, S Lam, CW Chan, AYW	2012	198
	A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia Journal:Hong Kong Medical Journal	Lee, HHC Lee, RSY Lai, CK Yuen, YP Siu, TS Chan, AYW Lam, CW	2010	149
	A novel mutation at a ligand-binding site of hypoxanthine-guanine phosphoribosyl transferase, p.Y105C (HPRTHongKong), in a Chinese teenager with recurrent gouty arthritis Journal:Clinica Chimica Acta	Lam, CW Lee, KP Ng, KF Siu, TS Chan, HM Tam, S	2007
	A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome Journal:Clinica Chimica Acta	Lam, CW Kong, APS Tsui, TKC Ozaki, R Chan, HM Tong, SF Siu, TS Tam, S Chan, JCN	2008	189
	Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient Journal:Clinica Chimica Acta	Cho, SY Siu, TS Ma, O Tam, S Lam, CW	2013
	Role of postmortem genetic testing demonstrated in a case of glutaric aciduria type II Journal:Diagnostic Molecular Pathology	Lee, HCH Lai, CK Siu, TS Yuen, YP Chan, KY Chan, AYW Tam, S Mak, CM Lam, CW	2010	141
	The variability of the hepatitis B virus genome: Statistical analysis and biological implications Journal:Molecular Biology and Evolution	Lauder, IJ Lin, HJ Lau, JYN Siu, TS Lai, CL	1993

Showing results 14 to 24 of 24 < previous