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Showing results 6 to 19 of 19 < previous

	Title	Author(s)	Issue Date
	Development of locked nucleic acid PCR technique for detecting circulating EBV DNA with dramatic enhancement in sensitivity in NPC patients Proceeding/Conference:GRC on Nasopharyngeal Carcinoma	Yip, TTC Kwok, HYY Wong, BMY You, SSY Fong, AHW Cheng, WW Lai, C Shek, CC Leung, KH Chiang, AKS Hui, KF Ma, VVS Lung, ML Ngan, RKC	2016
	Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria Journal:Hong Kong Medical Journal	Au, KM Lai, CK Yuen, YP Shek, CC Lam, CW Chan, AYW	2003
	DNA-based diagnosis of thyroid hormone resistance syndrome: A novel THRB mutation associated with mild resistance to thyroid hormone Journal:Clinica Chimica Acta	Lam, CW Chan, AOK Tong, SF Shek, CC Sau, CT	2005
	Epidemiology and Trends of Infective Meningitis in Neonates and Infants Less than 3 Months Old in Hong Kong Journal:International Journal of Infectious Diseases	Wong, CH Rosa Duque, J Wong, JSC Chan, CMV Lam, CSI Fu, YM Cheong, KN Chua, GT Lee, PP Ip, P Ho, MHK Wong, ICK Chan, GCF Leung, WH Lee, SL Lee, KP Shek, CC Wong, MSR Wong, MSC Lau, YL Kwan, MYW	2021
	Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a Journal:Clinical Genetics	Lam, CW But, WM Shek, CC Tong, SF Chan, YS Choy, KW Tse, WY Pang, CP Hjelm, NM	1998
	Independent association of serum vitamin D with anti-Mullerian hormone levels in women with polycystic ovary syndrome Journal:Clinical Endocrinology	Wong, HYQ Li, RHW Lam, KSL Tam, S Shek, CC Lee, VCY Yeung, WSB Ho, PC Ng, EHY	2018
	Infants born to mothers with severe acute respiratory syndrome. Journal:Pediatrics	Shek, CC Ng, PC Fung, GP Cheng, FW Chan, PK Peiris, MJ Lee, KH Wong, SF Cheung, HM Li, AM Hon, EK Yeung, CK Chow, CB Tam, JS Chiu, MC Fok, TF	2003
	Isolated 17,20-lyase deficiency in a Hong Kong Chinese patient with a novel nonsense mutation in the CYB5A gene Proceeding/Conference:Asia-Pacific Conference on Human Genetics, APCHG 2010	Chan, AOK Yeung, TWY Li, RHW Ng, EHY Ho, PC Lai, PS Shek, CC	2010
	Normal cord blood thyroid-stimulating hormone in a child with resistance to thyroid hormone Journal:Neuroembryology and Aging	Chan, AOK Lam, CW Lo, IFM Lam, STS Shek, CC Tiu, SC Tong, SF	2005
	Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC Journal:Clinical Chemistry	Lam, CW Poon, PMK Tong, SF Lo, AWI Lai, CK Choi, KL Tiu, SC Chan, YW Shek, CC	2001
	A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI Journal:Chinese Medical Journal	Lam, CW Chan, AOK Lai, CK Chan, WH Chan, YW Shek, CC Tong, SF	2004
	Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity Journal:Clinica Chimica Acta	OnKei Chan, A Lam, CW Tong, SF Man Tung, C Yung, K Chan, YW Au, KM Yuen, YP Hung, CT Ng, KP Shek, CC	2005
	Steroid 5α-reductase 2 deficiency in two generations of a non-consaguineous Chinese family Journal:Journal of Pediatric Endocrinology and Metabolism	Lee, CY Lam, CW Shek, CC	2003
	The first pilot study of expanded newborn screening for inborn errors of metabolism and survey of related knowledge and opinions of health care professionals in Hong Kong Journal:Hong Kong Medical Journal	Mak, CM Law, EC Lee, HH Siu, WK Chow, KM Au Yeung, SK Ngan, HYS Tse, NK Kwong, NS Chan, GC Lee, KW Chan, WP Wong, SF Tang, MH Kan, AS Hui, AP So, PL Shek, CC Lee, RS Wong, KY Yau, EK Poon, KH Siu, S Poon, GW Kwok, AM Ng, JW Yim, VC Ma, GG Chu, CH Tong, TY Chong, YK Chen, SP Ching, CK Chan, AO Tam, S Lau, RL Ng, WF Lee, KC Chan, AY Lam, CW	2018

Showing results 6 to 19 of 19 < previous