Chong SS - Search Results

1

A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia.

Tan AS, Quah TC, Low PS, Chong SS. Tan AS, et al. Among authors: chong ss. Blood. 2001 Jul 1;98(1):250-1. doi: 10.1182/blood.v98.1.250. Blood. 2001. PMID: 11439976 Free article. No abstract available.

2

A molecular epidemiologic study of thalassemia using newborns' cord blood in a multiracial Asian population in Singapore: results and recommendations for a population screening program.

Kham SK, Quah TC, Loong AM, Tan PL, Fraser A, Chong SS, Yeoh AE. Kham SK, et al. Among authors: chong ss. J Pediatr Hematol Oncol. 2004 Dec;26(12):817-9. J Pediatr Hematol Oncol. 2004. PMID: 15591902

3

Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.

Chong SS, Boehm CD, Higgs DR, Cutting GR. Chong SS, et al. Blood. 2000 Jan 1;95(1):360-2. Blood. 2000. PMID: 10607725 Free article.

4

Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.

Zhao M, Chen M, Tan ASC, Cheah FSH, Mathew J, Wong PC, Chong SS. Zhao M, et al. Among authors: chong ss. J Thromb Haemost. 2017 Jul;15(7):1473-1483. doi: 10.1111/jth.13685. Epub 2017 Apr 28. J Thromb Haemost. 2017. PMID: 28345288 Free article.

5

Spinocerebellar ataxia type 2 with focal epilepsy--an unusual association.

Tan NC, Zhou Y, Tan AS, Chong SS, Lee WL. Tan NC, et al. Among authors: chong ss. Ann Acad Med Singap. 2004 Jan;33(1):103-6. Ann Acad Med Singap. 2004. PMID: 15008574 Free article.

6

Simplified multiplex-PCR diagnosis of common southeast asian deletional determinants of alpha-thalassemia.

Chong SS, Boehm CD, Cutting GR, Higgs DR. Chong SS, et al. Clin Chem. 2000 Oct;46(10):1692-5. Clin Chem. 2000. PMID: 11017952 No abstract available.

7

The--THAI and--FIL determinants of alpha thalassemia in Taiwan.

Higgs DR, Ayyub H, Chong SS. Higgs DR, et al. Among authors: chong ss. Am J Hematol. 1999 Jan;60(1):80-1. doi: 10.1002/(sici)1096-8652(199901)60:1<80::aid-ajh17>3.0.co;2-w. Am J Hematol. 1999. PMID: 9883814 Free article. No abstract available.

8

Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay.

Zhou Y, Law HY, Boehm CD, Yoon CS, Cutting GR, Ng IS, Chong SS. Zhou Y, et al. Among authors: chong ss. J Med Genet. 2004 Apr;41(4):e45. doi: 10.1136/jmg.2003.012716. J Med Genet. 2004. PMID: 15060121 Free PMC article. No abstract available.

9

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophy.

Boehm CD, Cutting GR, Lachtermacher MB, Moser HW, Chong SS. Boehm CD, et al. Among authors: chong ss. Mol Genet Metab. 1999 Feb;66(2):128-36. doi: 10.1006/mgme.1998.2779. Mol Genet Metab. 1999. PMID: 10068516 Free article.

10

Preimplantation Genetic Testing of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease-Robust Tools for Direct and Indirect Detection of the ATXN3 (CAG)_n Repeat Expansion.

Lian M, Tan VJ, Taguchi R, Zhao M, Phang GP, Tan AS, Liu S, Lee CG, Chong SS. Lian M, et al. Among authors: chong ss. Int J Mol Sci. 2024 Jul 24;25(15):8073. doi: 10.3390/ijms25158073. Int J Mol Sci. 2024. PMID: 39125643 Free PMC article.

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