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Browsing by Author Tong, SF
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Showing results 49 to 58 of 58
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Title
Author(s)
Issue Date
Views
Organochlorine isotopic pattern-enhanced detection and quantification of triclosan and its metabolites in human serum by ultra-high-performance liquid chromatography/quadrupole time-of-flight/mass spectrometry
Journal:
Rapid Communications in Mass Spectrometry
Wu, JL
Leung, KF
Tong, SF
Lam, CW
2012
129
Pantothenate kinase-associated neurodegeneration in two Chinese children: Identification of a novel PANK2 gene mutation
Journal:
Hong Kong Medical Journal
Chan, KY
Lam, CW
Lee, LP
Tong, SF
Yuen, YP
2008
90
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2
Journal:
Journal of Hepatology
Lam, CW
Cheung, KM
Tsui, MS
Yan, MSC
Lee, CY
Tong, SF
2006
168
Persistent hypocalcaemia in a Chinese girl due to a novel de-novo activating mutation of the calciumsensing receptor gene
Journal:
Hong Kong Medical Journal
Wong, WC
Lam, CW
Tong, SF
Tong, CT
2011
149
Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography
Journal:
Prenatal Diagnosis
Lam, CW
Sin, SY
Lau, ET
Lam, YY
Poon, P
Tong, SF
2000
184
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b
Journal:
Clinica Chimica Acta
Lam, CW
Orrico, A
Yan, MSC
Law, TY
Galli, L
Benedetti, A
Tong, SF
Sorrentino, V
2006
179
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Journal:
Journal of medical genetics
Lam, CW
Yeung, WL
Ko, CH
Poon, PM
Tong, SF
Chan, KY
Lo, IF
Chan, LY
Hui, J
Wong, V
Pang, CP
Lo, YM
Fok, TF
2000
146
Sustainable Fashion Textiles Research on Innovative 3D Spacer Fabrics Comprising Shape Memory Alloy Wire for Pressure Reduction and Redistribution
Proceeding/Conference:
The Textile Institute World Conference
Tong, SF
Yip, J
Cheung, JPY
Yick, KL
Ng, SP
Yeung, KWK
2018
56
Two novel CLN2 gene mutations in an Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis [2]
Journal:
American Journal of Medical Genetics
Lam, CW
Poon, PMK
Tong, SF
Ko, CH
2001
183
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivation
Journal:
Clinica Chimica Acta
Cho, SY
Lam, CW
Tong, SF
Siu, CWK
2013
57
