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Advances in Clinical Chemistry
|
February 1, 2011
Microarrays for personalized genomic medicine
Ching-Wan Lam, Kin-Chong Lau, Sui-Fan Tong
Clinical Biochemistry
|
March 4, 2006
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays
Ching-Wan Lam, Ka-Fai To, Sui-Fan Tong
Rapid Communications in Mass Spectrometry : RCM
|
December 17, 2011
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
Jian-lin Wu, Ka-Fai Leung, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 24, 2013
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivation
Sun Young Cho, Ching-wan Lam, Sui-Fan Tong, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Ching-Wan Lam, Anna Wai-Fun Cheng, Sui-Fan Tong, et al.
Brain & Development
|
December 27, 2005
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease
Wai Lan Yeung, Ching Wan Lam, Joannie Hui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 13, 2005
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Ching-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2005
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone
Ching-Wan Lam, Angel On-Kei Chan, Sui-Fan Tong, et al.
The Laryngoscope
|
July 28, 2011
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?
Yang Zha, Xing-ming Chen, Ching-wan Lam, et al.
Molecular Genetics and Metabolism
|
March 27, 2009
WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
Yuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
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of 3
Search research articles
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Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Advances in Clinical Chemistry
|
February 1, 2011
Microarrays for personalized genomic medicine
Ching-Wan Lam, Kin-Chong Lau, Sui-Fan Tong
Clinical Biochemistry
|
March 4, 2006
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays
Ching-Wan Lam, Ka-Fai To, Sui-Fan Tong
Rapid Communications in Mass Spectrometry : RCM
|
December 17, 2011
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
Jian-lin Wu, Ka-Fai Leung, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 24, 2013
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivation
Sun Young Cho, Ching-wan Lam, Sui-Fan Tong, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Ching-Wan Lam, Anna Wai-Fun Cheng, Sui-Fan Tong, et al.
Brain & Development
|
December 27, 2005
Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease
Wai Lan Yeung, Ching Wan Lam, Joannie Hui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 13, 2005
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Ching-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2005
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone
Ching-Wan Lam, Angel On-Kei Chan, Sui-Fan Tong, et al.
The Laryngoscope
|
July 28, 2011
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?
Yang Zha, Xing-ming Chen, Ching-wan Lam, et al.
Molecular Genetics and Metabolism
|
March 27, 2009
WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
Yuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
Page
of 3