Browsing by Author Tong, SF

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TitleAuthor(s)Issue Date
 
Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death
Journal:Chinese Medical Journal
Lam, CWLai, CKChow, CBTong, SFYuen, YPMak, YFChan, YW
2003
 
Evaluation of a new handheld biosensor for point-of-care testing of whole blood beta-hydroxybutyrate concentration.
Journal:Hong Kong medical journal = Xianggang yi xue za zhi / Hong Kong Academy of Medicine
Chiu, RWHo, CSTong, SFNg, KFLam, CW
2002
 
Fatal viral infection-associated encephalopathy in two Chinese boys: A genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants
Journal:Journal of Human Genetics
Mak, CMLam, CWFong, NCSiu, WKLee, HCHSiu, TSLai, CKLaw, CYTong, SFPoon, WTLam, DSYNg, HLYuen, YPTam, SQue, TLKwong, NSChan, AYW
2011
 
A frequent activated smoothened mutation in sporadic basal cell carcinomas
Journal:Oncogene
Lam, CWXie, JTo, KFNg, HKLee, KCYuen, NWFLim, PLChan, LYSTong, SFMccormick, F
1999
 
Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter disease
Journal:Brain and Development
Yeung, WLLam, CWHui, JTong, SFWu, SP
2006
 
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays
Journal:Clinical Biochemistry
Lam, CWTo, KFTong, SF
2006
 
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, CWBut, WMShek, CCTong, SFChan, YSChoy, KWTse, WYPang, CPHjelm, NM
1998
 
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria
Journal:Kidney International
Yuen, YPLam, CWLai, CKTong, SFLi, PSTam, SKwan, EYWChan, SYTsang, WKChan, KYMak, WLCheng, CWChan, YW
2006
 
Identification of RASSF1A modulated genes in nasopharyngeal carcinoma
Journal:Oncogene
Chow, LSNLam, CWChan, SYYTsao, SWTo, KFTong, SFHung, WKDammann, RHuang, DPLo, KW
2006
 
Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients?
Journal:Laryngoscope
Zha, YChen, XMLam, CWLee, SCTong, SFGao, ZQ
2011
 
Juvenile-onset glycogen storage disease type II with novel mutations in acid α-glucosidase gene
Journal:Neurology
Lam, CWYuen, YPChan, KYTong, SFLai, CKChow, TCLee, KCChan, YWMartiniuk, F
2003
 
Maternally inherited leigh syndrome: An unusual cause of infantile apnea
Journal:Sleep and Breathing
Chau, CSKKwok, KLNg, DKLam, CWTong, SFChan, YWSiu, WKYuen, YP
2010
 
MECP2 mutation in male patients with non-specific X-linked mental retardation
Journal:FEBS Letters
Orrico, ALam, CWGalli, LDotti, MTHayek, GTong, SFPoon, PMKZappella, MFederico, ASorrentino, V
2000
 
Microarrays for personalized genomic medicine
Journal:Advances in Clinical Chemistry
Lam, CWLau, KCTong, SF
2010
 
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Journal:Clinica Chimica Acta
Lam, CWYuen, YPCheng, WFChan, YWTong, SF
2006
 
Molecular basis of von Hippel-Lindau syndrome in Chinese patients
Journal:Chinese Medical Journal
Siu, WKMa, RCWLam, CWMak, CMYuen, YPLo, FMIChan, KWLam, SFLing, SCTong, SFSo, WYChow, CCTang, MHYTam, WHChan, AYW
2011
 
Molecular genetic analysis of a Chinese patient with Fabry disease
Journal:Chinese Medical Journal
Lam, CWMak, YTLo, YMDTong, SFTo, KFLai, FMM
2000
 
Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17α-hydroxylase deficiency
Journal:Molecular Genetics and Metabolism
Lam, CWArlt, WChan, CKHonour, JWLin, CJTong, SFChoy, KWMiller, WL
2001
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, JYYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2)
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, STYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
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