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S F Tong

Showing results (11-20 of 35) with videos related to

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Journal of Tropical Pediatrics|November 28, 2007
The accuracy of mother's touch to detect fever in children: a systematic reviewC L Teng, C J Ng, H Nik-Sherina, et al.
Clinical Genetics|August 26, 1998
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 1aC W Lam, M H Liang, C P Pang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 11, 2002
Evaluation of a new handheld biosensor for point-of-care testing of whole blood beta-hydroxybutyrate concentrationR W K Chiu, C S Ho, S F Tong, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatographyC W Lam, S Y Sin, E T Lau, et al.
Human Mutation|June 30, 2000
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1bC W Lam, K Y Chan, S F Tong, et al.
Chinese Medical Journal|January 5, 2002
Molecular genetic analysis of a Chinese patient with Fabry diseaseC W Lam, Y T Mak, Y M Lo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 2001
Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donorC W Lam, Y P Yuen, C K Lai, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|April 5, 2007
A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiencyRonald C W Ma, C W Lam, W B Chan, et al.
FEBS Letters|September 29, 2000
MECP2 mutation in male patients with non-specific X-linked mental retardationA Orrico, C Lam, L Galli, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of Tropical Pediatrics|November 28, 2007
The accuracy of mother's touch to detect fever in children: a systematic reviewC L Teng, C J Ng, H Nik-Sherina, et al.
Clinical Genetics|August 26, 1998
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 1aC W Lam, M H Liang, C P Pang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 11, 2002
Evaluation of a new handheld biosensor for point-of-care testing of whole blood beta-hydroxybutyrate concentrationR W K Chiu, C S Ho, S F Tong, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatographyC W Lam, S Y Sin, E T Lau, et al.
Human Mutation|June 30, 2000
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1bC W Lam, K Y Chan, S F Tong, et al.
Chinese Medical Journal|January 5, 2002
Molecular genetic analysis of a Chinese patient with Fabry diseaseC W Lam, Y T Mak, Y M Lo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 2001
Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donorC W Lam, Y P Yuen, C K Lai, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|April 5, 2007
A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiencyRonald C W Ma, C W Lam, W B Chan, et al.
FEBS Letters|September 29, 2000
MECP2 mutation in male patients with non-specific X-linked mental retardationA Orrico, C Lam, L Galli, et al.
Pageof 4