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Ching-Wan Lam

Showing results (61-70 of 179) with videos related to

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Chinese Medical Journal|January 4, 2007
Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncopeNgai-Shing Mok, Ching-Wan Lam, Nai-Chung Fong, et al.
Molecular Genetics and Metabolism|March 27, 2009
WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
Molecular Genetics and Metabolism|November 1, 2002
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
Pediatrics and Neonatology|July 8, 2009
Glycogen storage disease type Ib: the first case in TaiwanHui-Ju Hsiao, Hsiu-Hao Chang, Wuh-Liang Hwu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 18, 2004
Diagnostic value of pleural fluid adenosine deaminase activity in tuberculous pleurisyMo-Lung Chen, Wai-Cho Yu, Ching-Wan Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 13, 2006
DNA-based diagnosis of mucolipidosis type IIIA and mucopolysacchariodisis type VI in a Chinese family: a chance of 1 in 7.6 trillionChing-Wan Lam, Matthew Shu-Ching Yan, Chi-Kong Li, et al.
Rapid Communications in Mass Spectrometry : RCM|February 19, 2013
Electrospray ionization on porous spraying tips for direct sample analysis by mass spectrometry: enhanced detection sensitivity and selectivity using hydrophobic/hydrophilic materials as spraying tipsMelody Yee-Man Wong, Ho-Wai Tang, Sin-Heng Man, et al.
The Journal of Investigative Dermatology|January 19, 2005
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarrayChing-Wan Lam, Kitty Kit-Ting Cheung, Nai-Ming Luk, et al.
Behavioural Brain Research|November 1, 2015
Unmasking a novel disease gene NEO1 associated with autism spectrum disorders by a hemizygous deletion on chromosome 15 and a functional polymorphismWai-Kwan Siu, Ching-Wan Lam, Wei-Wei Gao, et al.
Journal of Hepatology|November 18, 2005
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2Ching-Wan Lam, Ka-Ming Cheung, Man-Shan Tsui, et al.
Pageof 18

Showing results (61-70 of 179) with videos related to

Sort By:
Pageof 18
Chinese Medical Journal|January 4, 2007
Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncopeNgai-Shing Mok, Ching-Wan Lam, Nai-Chung Fong, et al.
Molecular Genetics and Metabolism|March 27, 2009
WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
Molecular Genetics and Metabolism|November 1, 2002
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
Pediatrics and Neonatology|July 8, 2009
Glycogen storage disease type Ib: the first case in TaiwanHui-Ju Hsiao, Hsiu-Hao Chang, Wuh-Liang Hwu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 18, 2004
Diagnostic value of pleural fluid adenosine deaminase activity in tuberculous pleurisyMo-Lung Chen, Wai-Cho Yu, Ching-Wan Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 13, 2006
DNA-based diagnosis of mucolipidosis type IIIA and mucopolysacchariodisis type VI in a Chinese family: a chance of 1 in 7.6 trillionChing-Wan Lam, Matthew Shu-Ching Yan, Chi-Kong Li, et al.
Rapid Communications in Mass Spectrometry : RCM|February 19, 2013
Electrospray ionization on porous spraying tips for direct sample analysis by mass spectrometry: enhanced detection sensitivity and selectivity using hydrophobic/hydrophilic materials as spraying tipsMelody Yee-Man Wong, Ho-Wai Tang, Sin-Heng Man, et al.
The Journal of Investigative Dermatology|January 19, 2005
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarrayChing-Wan Lam, Kitty Kit-Ting Cheung, Nai-Ming Luk, et al.
Behavioural Brain Research|November 1, 2015
Unmasking a novel disease gene NEO1 associated with autism spectrum disorders by a hemizygous deletion on chromosome 15 and a functional polymorphismWai-Kwan Siu, Ching-Wan Lam, Wei-Wei Gao, et al.
Journal of Hepatology|November 18, 2005
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2Ching-Wan Lam, Ka-Ming Cheung, Man-Shan Tsui, et al.
Pageof 18