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Sui-Fan Tong

Research Profile

Procedures

Physiology

Living Beings

Chemicals & Drugs

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Hong Kong

Disorders

Glycogen Storage Disease Type I

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Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Publications

TOP 3
Yang Zha; Xing-ming Chen; Ching-Wan Lam; Soo-Chin Lee; Sui-Fan Tong; Zhi-qiang Gao
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?
Wai-Kwan Siu; Ronald Ching-Wan Ma; Ching-Wan Lam; Chloe Miu Mak; Yuet-Ping Yuen; Fai-man Ivan Lo; Kin-Wah Chan; Siu-Fung Lam; Siu-Cheung Ling; Sui-Fan Tong; Wing-Yee So; Chun-Chung Chow; Mary Hoi-Yin Tang; Wing-Hung Tam; Albert Yan-Wo Chan
Molecular basis of von Hippel-Lindau syndrome in Chinese patients.
Christy Shuk-kuen Chau; Ka-Li Kwok; Daniel K Ng; Ching-Wan Lam; Sui-Fan Tong; Yan-Wo Chan; Wai-Kwan Siu; Yuet-Ping Yuen
Maternally inherited Leigh syndrome: an unusual cause of infantile apnea.

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All Publications

2011: Yang Zha; Xing-ming Chen; Ching-Wan Lam; Soo-Chin Lee; Sui-Fan Tong; Zhi-qiang Gao
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?
The Laryngoscope 2011;121(8):1760-4.
2011: Wai-Kwan Siu; Ronald Ching-Wan Ma; Ching-Wan Lam; Chloe Miu Mak; Yuet-Ping Yuen; Fai-man Ivan Lo; Kin-Wah Chan; Siu-Fung Lam; Siu-Cheung Ling; Sui-Fan Tong; Wing-Yee So; Chun-Chung Chow; Mary Hoi-Yin Tang; Wing-Hung Tam; Albert Yan-Wo Chan
Molecular basis of von Hippel-Lindau syndrome in Chinese patients.
Chinese medical journal 2011;124(2):237-41.
2010: Christy Shuk-kuen Chau; Ka-Li Kwok; Daniel K Ng; Ching-Wan Lam; Sui-Fan Tong; Yan-Wo Chan; Wai-Kwan Siu; Yuet-Ping Yuen
Maternally inherited Leigh syndrome: an unusual cause of infantile apnea.
Sleep & breathing = Schlaf & Atmung 2010;14(2):161-5.
2010: C M Mak; Ching-Wan Lam; T S Siu; Kwok-Yin Chan; W K Siu; W L Yeung; J Hui; V C N Wong; L C K Low; C H Ko; C W Fung; S P Chen; Yuet-Ping Yuen; H C Lee; E Yau; B Chan; Sui-Fan Tong; S Tam; Yan-Wo Chan
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.
Molecular genetics and metabolism 2010;99(4):431-3.
2010: Ching-Wan Lam; Kin-Chong Lau; Sui-Fan Tong
Microarrays for personalized genomic medicine.
Advances in clinical chemistry 2010;52():1-18.
2008: Ching-Wan Lam; Alice P S Kong; Teresa K C Tsui; Risa Ozaki; Ho-Ming Chan; Sui-Fan Tong; Tak-Shing Siu; Sidney Tam; Juliana C N Chan
A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome.
Clinica chimica acta; international journal of clinical chemistry 2008;398(1-2):157-8.
2008: Chloe Miu Mak; Ching-Wan Lam; Sidney Tam; Ching-Lung Lai; Lik-Yuen Chan; Sheung-Tat Fan; Yu-Lung Lau; Sik-To Lai; Jak-Yiu Lai; Patrick Yuen; Joannie Hui; Chun-Cheung Fu; Ka Sing Wong; Wing-Lai Mak; Kong Tze; Sui-Fan Tong; Abby Lau; Nancy Leung; Aric Hui; Ka-Ming Cheung; Chun-Hung Ko; Yiu-Ki Chan; Oliver Ma; Tai Nin Chau; Alexander Chiu; Yan-Wo Chan
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(1):55-63.
2007: A O K Chan; Ching-Wan Lam; Sui-Fan Tong; C M Tung; Kwok Yung; Yan-Wo Chan; Kam-Ming Au; Yuet-Ping Yuen; Chi-Tim Hung; Kin-Pong Ng; Chi-Chung Shek
Gene symbol: BCHE.
Human genetics 2007;121(2):289.
2007: A O K Chan; Ching-Wan Lam; Sui-Fan Tong; M T Cheng; Kwok Yung; Yan-Wo Chan; Kam-Ming Au; Yuet-Ping Yuen; Chi-Tim Hung; Kin-Pong Ng; Chi-Chung Shek
Gene symbol: BCHE.
Human genetics 2007;121(2):288.
2007: Ching-Wan Lam; Matthew Shu-Ching Yan; Chi kong Li; Kin-Chong Lau; Sui-Fan Tong; Hoi-Yin Tang
DNA-based diagnosis of mucolipidosis type IIIA and mucopolysacchariodisis type VI in a Chinese family: a chance of 1 in 7.6 trillion.
Clinica chimica acta; international journal of clinical chemistry 2007;376(1-2):250-2.
2007: Ching-Wan Lam; Sui-Fan Tong; Keong Wong; Y F Luo; Hoi-Yin Tang; Shau-Yin Ha; Michael H M Chan
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity.
Journal of human genetics 2007;52(1):98-101.
2007: Yuet-Ping Yuen; Chi-Kong Lai; Yan-Wo Chan; Ching-Wan Lam; Sui-Fan Tong; Kwok-Yin Chan
DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delay.
Clinica chimica acta; international journal of clinical chemistry 2007;375(1-2):171-2.
2006: Ching-Wan Lam; Matthew Shu-Ching Yan; Tat-Yin Law; Sui-Fan Tong; Alfredo Orrico; Lucia Galli; Vincenzo Sorrentino; Angelo Benedetti
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b.
Clinica chimica acta; international journal of clinical chemistry 2006;374(1-2):147-8.
2006: Wai Lan Yeung; Ching-Wan Lam; Joannie Hui; Sui-Fan Tong; Shun Ping Wu
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease.
Brain & development 2006;28(6):389-91.
2006: Ching-Wan Lam; Ka-Fai To; Sui-Fan Tong
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays.
Clinical biochemistry 2006;39(3):187-90.
2006: Wing-Tat Poon; Kam-Ming Au; Yan-Wo Chan; Kwok-Yin Chan; Chun-Bong Chow; Sui-Fan Tong; Ching-Wan Lam
Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia.
Clinica chimica acta; international journal of clinical chemistry 2006;364(1-2):361-2.
2006: Ching-Wan Lam; Yuet-Ping Yuen; Wai-Fun Cheng; Yan-Wo Chan; Sui-Fan Tong
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.
Clinica chimica acta; international journal of clinical chemistry 2006;364(1-2):256-9.
2006: Yuet-Ping Yuen; C-W Lam; Chi-Kong Lai; Sui-Fan Tong; P-S Li; S Tam; E Y-W Kwan; S-Y Chan; W-K Tsang; Kwok-Yin Chan; W-L Mak; C-W Cheng; Yan-Wo Chan
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria.
Kidney international 2006;69(1):123-8.
2006: Ching-Wan Lam; Ka-Ming Cheung; Man-Shan Tsui; Matthew Shu-Ching Yan; Ching-Yin Lee; Sui-Fan Tong
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2.
Journal of hepatology 2006;44(1):240-2.
2005: Ching-Wan Lam; Ka-Fai Lee; A O K Chan; Priscilla M K Poon; Tak-Yin Law; Sui-Fan Tong
Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemia.
Clinica chimica acta; international journal of clinical chemistry 2005;360(1-2):167-72.
2005: Ching-Wan Lam; Angel On-Kei Chan; Sui-Fan Tong; Chi-Chung Shek; Sau Cheung Tiu
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone.
Clinica chimica acta; international journal of clinical chemistry 2005;358(1-2):55-9.
2005: Ching-Wan Lam; Kitty Kit-Ting Cheung; Nai-Ming Luk; Shirley Wen Chan; Kuen Kong Lo; Sui-Fan Tong
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarray.
The Journal of investigative dermatology 2005;124(1):87-91.
2005: Angel On-Kei Chan; Ching-Wan Lam; Sui-Fan Tong; Cheng Man Tung; Kwok Yung; Yan-Wo Chan; Kam-Ming Au; Yuet-Ping Yuen; Chi-Tim Hung; Kin-Pong Ng; Chi-Chung Shek
Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity.
Clinica chimica acta; international journal of clinical chemistry 2005;351(1-2):155-9.
2004: Ching-Wan Lam; A O K Chan; Chi-Kong Lai; Wai-hung Chan; Yan-Wo Chan; Chi-Chung Shek; Sui-Fan Tong
A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI.
Chinese medical journal 2004;117(12):1850-2.
2004: Ching-Wan Lam; Allen Ting-Chun Lee; Yuen-yu Lam; Tak-Wai Wong; Tony Wing-Lai Mak; Wai-Ching Fung; Kwok-Chiu Chan; Che-Shun Ho; Sui-Fan Tong
DNA-based subtyping of glycogen storage disease type III: mutation and haplotype analysis of the AGL gene in Chinese.
Molecular genetics and metabolism 2004;83(3):271-5.
2004: Yuet-Ping Yuen; Chi-Kong Lai; Gensy M W Tong; Ping-Nam Wong; Francis Kim-Ming Wong; Siu-Ka Mak; Kin-Yee Lo; Andrew K M Wong; Sui-Fan Tong; Yan-Wo Chan; Ching-Wan Lam
Novel mutations of the AGXT gene causing primary hyperoxaluria type 1.
Journal of nephrology 2004;17(3):436-40.
2003: Ching-Wan Lam; Chi-Kong Lai; Chun-Bong Chow; Sui-Fan Tong; Yuet-Ping Yuen; Yuen Fun Mak; Yan-Wo Chan
Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death.
Chinese medical journal 2003;116(7):1110-2.
2003: Ching-Wan Lam; Yuet-Ping Yuen; Kwok-Yin Chan; Sui-Fan Tong; Chi-Kong Lai; T C Chow; K C Lee; Yan-Wo Chan; F Martiniuk
Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase gene.
Neurology 2003;60(4):715-7.
2002: Yuet-Ping Yuen; Wai-Fun Cheng; Sui-Fan Tong; Yuk-Tat Chan; Yan-Wo Chan; Ching-Wan Lam
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b.
Molecular genetics and metabolism 2002;77(3):249-51.
2002: Rossa W K Chiu; C S Ho; Sui-Fan Tong; K F Ng; Ching-Wan Lam
Evaluation of a new handheld biosensor for point-of-care testing of whole blood beta-hydroxybutyrate concentration.
Hong Kong medical journal = Xianggang yi xue za zhi / Hong Kong Academy of Medicine 2002;8(3):172-6.
2002: Ching-Wan Lam; Chi-Yan Leung; Kam-Cheong Lee; Jingwu Xie; Fai-man Ivan Lo; Tak-Shing Au; Sui-Fan Tong; Miu-Kuen Poon; Loi-Yuen Chan; Nai-Ming Luk
Novel mutations in the PATCHED gene in basal cell nevus syndrome.
Molecular genetics and metabolism 2002;76(1):57-61.
2002: Tao Yang; Ching-Wan Lam; Man Wo Tsang; Sui-Fan Tong; Grace Y W Kam; Lisa Y S Chan; Priscilla M K Poon; Xiangqian Wu; Chi Pui Pang
Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetes.
Chinese medical journal 2002;115(5):753-8.
2002: Ching-Wan Lam; Anna Wai-Fun Cheng; Sui-Fan Tong; Yan-Wo Chan
Novel donor splice site mutation of ABCG5 gene in sitosterolemia.
Molecular genetics and metabolism 2002;75(2):178-80.
2002: Ching-Wan Lam; Chi-Keung Li; Chi-Kong Lai; Sui-Fan Tong; Kwok-Yin Chan; Grace Sui-Fun Ng; Yuet-Ping Yuen; Anna Wai-Fun Cheng; Yan-Wo Chan
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Molecular genetics and metabolism 2002;75(1):91-5.
2001: Ching-Wan Lam; Yuet-Ping Yuen; Chi-Kong Lai; Sui-Fan Tong; L K Lau; KL Tong; Yan-Wo Chan
Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2001;38(6):1307-10.
2001: Ching-Wan Lam; K N Hui; Priscilla M K Poon; Nai-Ming Luk; Yuet-Ping Yuen; Sui-Fan Tong; Chi-Kong Lai; Yan-Wo Chan; Kuen Kong Lo
Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatography.
Clinica chimica acta; international journal of clinical chemistry 2001;305(1-2):197-200.
2001: Ching-Wan Lam; W Arlt; C K Chan; John HONOUR; C J Lin; Sui-Fan Tong; K W Choy; W L Miller
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiency.
Molecular genetics and metabolism 2001;72(3):254-9.
2001: C W Lam; Priscilla M K Poon; Sui-Fan Tong; C H Ko
Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis.
American journal of medical genetics 2001;99(2):161-3.
2001: Ching-Wan Lam; Priscilla M K Poon; Sui-Fan Tong; A W Lo; Chi-Kong Lai; Kin-Lam Choi; Sau-Cheung Tiu; Yan-Wo Chan; Chi-Chung Shek
Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC.
Clinical chemistry 2001;47(2):343-6.
2000: Ching-Wan Lam; Wai Lan Yeung; C H Ko; Priscilla M K Poon; Sui-Fan Tong; K Y Chan; I F Lo; L Y Chan; J Hui; V Wong; Chi Pui Pang; Y M Dennis Lo; T F Fok
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Journal of medical genetics 2000;37(12):E41.
2000: Tao Yang; Ching-Wan Lam; Man Wo Tsang; Sui-Fan Tong; Lisa Y S Chan; Grace Y W Kam; Priscilla M K Poon; Xiang-Qian Wu; Chi Pui Pang
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.
Human mutation 2000;16(4):375.
2000: Alfredo Orrico; C Lam; Lucia Galli; Maria Teresa Dotti; Giuseppe Hayek; Sui-Fan Tong; Priscilla M K Poon; Michele Zappella; A Federico; Vincenzo Sorrentino
MECP2 mutation in male patients with non-specific X-linked mental retardation.
FEBS letters 2000;481(3):285-8.
2000: Ching-Wan Lam; S Y Sin; E T Lau; Yuen-yu Lam; P Poon; Sui-Fan Tong
Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography.
Prenatal diagnosis 2000;20(9):765-8.
2000: Ching-Wan Lam; Kwok-Yin Chan; Sui-Fan Tong; B Y Chan; Y T Chan; Yan-Wo Chan
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b.
Human mutation 2000;16(1):94.
2000: Ching-Wan Lam; Y T Mak; Y M Lo; Sui-Fan Tong; K F To; F M Lai
Molecular genetic analysis of a Chinese patient with Fabry disease.
Chinese medical journal 2000;113(2):186-8.
1999: Ching-Wan Lam; B Y Chan; Sui-Fan Tong
Definition of the correct sequence in the donor splice site of intron 2 in the human glucose 6-phosphate translocase gene.
FEBS letters 1999;445(2-3):449-50.
1999: Ching-Wan Lam; J Xie; Ka-Fai To; H K Ng; K C Lee; N W Yuen; P L Lim; L Y Chan; Sui-Fan Tong; F McCormick
A frequent activated smoothened mutation in sporadic basal cell carcinomas.
Oncogene 1999;18(3):833-6.
1998: Ching-Wan Lam; Minna Liang; C P Pang; Sui-Fan Tong; L J Wong
A novel DraI polymorphism in the 3' untranslated region of human glucose-6-phosphatase gene: useful for carrier detection and prenatal diagnosis of glycogen storage disease type 1a.
Clinical genetics 1998;53(6):502-3.
1998: C P Pang; J Zhang; J Woo; D Chan; L K Law; Sui-Fan Tong; T Kwok; R Kay
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 1998;13(3):529-32.
1998: Ching-Wan Lam; Wai-man But; Chi-Chung Shek; Sui-Fan Tong; Y S Chan; K W Choy; W Y Tse; Chi Pui Pang; NM Hjelm
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a.
Clinical genetics 1998;53(3):184-90.