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	Title	Author(s)	Issue Date
	Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy Journal:Clinica Chimica Acta	Law, CY Chang, T Cho, SY Yau, EK Ng, GS Fong, NC Lam, CW	2015
	Genome-wide copy number variation study in anorectal malformations Journal:Human Molecular Genetics	Wong, EHM Cui, L Ng, CL Tang, CSM Liu, X So, MT Yip, BHK Cheng, G Zhang, R Tang, WK Yang, W Lau, YL Baum, L Kwan, P Sun, LD Zuo, XB Ren, YQ Yin, XY Miao, X Liu, JJ Lui, VCH Ngan, ESW Yuan, ZW Zhang, SW Xia, JL Wang, HL Sun, XB Wang, RY Chang, T Chan, IHY Chung, HY Zhang, XJ Wong, KKY Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2013
	High Rates of Viral Suppression After Long-term Entecavir Treatment of Asian Patients With Hepatitis B e Antigen-Positive Chronic Hepatitis B Journal:Clinical Gastroenterology and Hepatology	Pan, CQ Tong, M Kowdley, KV Hu, K Chang, T Lai, C Yoon, SK Lee, SS Cohen, D Tang, H Tsai, N	2012
	The Utilization Patterns, Functions and Outcomes of Medical social Services at Accident and Emergency Department in Hospitals in Hong Kong: A Preliminary Study	Wong, DFK Chan, CLW Law, CK Wong, TW Au, TYW Chang, T Fu, K Lee, ML Leung, D Tam, V Tsoi, YK	2000

Showing results 1 to 4 of 4