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S F Tong

Showing results (21-30 of 35) with videos related to

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Molecular Genetics and Metabolism|March 13, 2001
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiencyC W Lam, W Arlt, C K Chan, et al.
The Medical Journal of Malaysia|May 6, 2017
Feasibility of Implementing Chronic Care Model in the Malaysian Public Primary Care SettingF Ariffin, A S Ramli, M H Daud, et al.
Neurology|February 26, 2003
Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase geneC W Lam, Y P Yuen, K Y Chan, et al.
Human Mutation|October 3, 2000
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA geneT Yang, C W Lam, M W Tsang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 16, 2001
Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatographyC W Lam, K N Hui, P M Poon, et al.
Clinical Chemistry|February 13, 2001
Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLCC W Lam, P M Poon, S F Tong, et al.
Clinical Genetics|June 18, 1998
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1aC W Lam, W M But, C C Shek, et al.
Oncogene|February 16, 1999
A frequent activated smoothened mutation in sporadic basal cell carcinomasC W Lam, J Xie, K F To, et al.
Oncogene|August 24, 2005
Identification of RASSF1A modulated genes in nasopharyngeal carcinomaL S-N Chow, C-W Lam, S Y-Y Chan, et al.
Human Genetics|June 29, 2007
Gene symbol: BCHEA O K Chan, C W Lam, S F Tong, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Molecular Genetics and Metabolism|March 13, 2001
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiencyC W Lam, W Arlt, C K Chan, et al.
The Medical Journal of Malaysia|May 6, 2017
Feasibility of Implementing Chronic Care Model in the Malaysian Public Primary Care SettingF Ariffin, A S Ramli, M H Daud, et al.
Neurology|February 26, 2003
Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase geneC W Lam, Y P Yuen, K Y Chan, et al.
Human Mutation|October 3, 2000
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA geneT Yang, C W Lam, M W Tsang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 16, 2001
Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatographyC W Lam, K N Hui, P M Poon, et al.
Clinical Chemistry|February 13, 2001
Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLCC W Lam, P M Poon, S F Tong, et al.
Clinical Genetics|June 18, 1998
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1aC W Lam, W M But, C C Shek, et al.
Oncogene|February 16, 1999
A frequent activated smoothened mutation in sporadic basal cell carcinomasC W Lam, J Xie, K F To, et al.
Oncogene|August 24, 2005
Identification of RASSF1A modulated genes in nasopharyngeal carcinomaL S-N Chow, C-W Lam, S Y-Y Chan, et al.
Human Genetics|June 29, 2007
Gene symbol: BCHEA O K Chan, C W Lam, S F Tong, et al.
Pageof 4