Tong SF - Search Results

1

Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.

Yang T, Lam CW, Tsang MW, Tong SF, Chan LY, Kam GY, Poon PM, Wu XQ, Pang CP. Yang T, et al. Among authors: tong sf. Hum Mutat. 2000 Oct;16(4):375. doi: 10.1002/1098-1004(200010)16:4<375::AID-HUMU20>3.0.CO;2-F. Hum Mutat. 2000. PMID: 11013458 No abstract available.

2

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.

Lam CW, Liang MH, Pang CP, Tong SF, Wong LJ. Lam CW, et al. Among authors: tong sf. Clin Genet. 1998 Jun;53(6):502-3. doi: 10.1111/j.1399-0004.1998.tb02604.x. Clin Genet. 1998. PMID: 9712544 No abstract available.

3

A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b.

Lam CW, Chan KY, Tong SF, Chan BY, Chan YT, Chan YW. Lam CW, et al. Among authors: tong sf. Hum Mutat. 2000 Jul;16(1):94. doi: 10.1002/1098-1004(200007)16:1<94::AID-HUMU26>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 10874322 No abstract available.

4

Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC.

Lam CW, Poon PM, Tong SF, Lo AW, Lai CK, Choi KL, Tiu SC, Chan YW, Shek CC. Lam CW, et al. Among authors: tong sf. Clin Chem. 2001 Feb;47(2):343-6. Clin Chem. 2001. PMID: 11159788 No abstract available.

5

Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a.

Lam CW, But WM, Shek CC, Tong SF, Chan YS, Choy KW, Tse WY, Pang CP, Hjelm NM. Lam CW, et al. Among authors: tong sf. Clin Genet. 1998 Mar;53(3):184-90. doi: 10.1111/j.1399-0004.1998.tb02674.x. Clin Genet. 1998. PMID: 9630072

6

Definition of the correct sequence in the donor splice site of intron 2 in the human glucose 6-phosphate translocase gene.

Lam CW, Chan BY, Tong SF. Lam CW, et al. Among authors: tong sf. FEBS Lett. 1999 Feb 26;445(2-3):449-50. doi: 10.1016/s0014-5793(99)00167-2. FEBS Lett. 1999. PMID: 10094505 Free article. No abstract available.

7

Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography.

Lam CW, Sin SY, Lau ET, Lam YY, Poon P, Tong SF. Lam CW, et al. Among authors: tong sf. Prenat Diagn. 2000 Sep;20(9):765-8. doi: 10.1002/1097-0223(200009)20:9<765::aid-pd893>3.0.co;2-s. Prenat Diagn. 2000. PMID: 11015710

8

Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatography.

Lam CW, Hui KN, Poon PM, Luk NM, Yuen YP, Tong SF, Lai CK, Chan YW, Lo KK. Lam CW, et al. Among authors: tong sf. Clin Chim Acta. 2001 Mar;305(1-2):197-200. doi: 10.1016/s0009-8981(01)00382-5. Clin Chim Acta. 2001. PMID: 11249940 No abstract available.

9

Gene symbol: BCHE.

Chan AO, Lam CW, Tong SF, Tung CM, Yung K, Chan YW, Au KM, Yuen YP, Hung CT, Ng KP, Shek CC. Chan AO, et al. Among authors: tong sf. Hum Genet. 2007 Apr;121(2):289. Hum Genet. 2007. PMID: 17598228 No abstract available.

10

Pantothenate kinase-associated neurodegeneration in two Chinese children: identification of a novel PANK2 gene mutation.

Chan KY, Lam CW, Lee LP, Tong SF, Yuen YP. Chan KY, et al. Among authors: tong sf. Hong Kong Med J. 2008 Feb;14(1):70-3. Hong Kong Med J. 2008. PMID: 18239249 Free article.

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