Chieng WS - Search Results

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Recurring MLH1 deleterious mutations in unrelated Chinese Lynch syndrome families in Singapore.

Yap HL, Chieng WS, Lim JR, Lim RS, Soo R, Guo J, Lee SC. Yap HL, et al. Among authors: chieng ws. Fam Cancer. 2009;8(2):85-94. doi: 10.1007/s10689-008-9209-5. Epub 2008 Aug 23. Fam Cancer. 2009. PMID: 18726168

Establishing a cancer genetics programme in Asia - the singapore experience.

Chieng WS, Lee SC. Chieng WS, et al. Hered Cancer Clin Pract. 2006 Jun 15;4(3):126-35. doi: 10.1186/1897-4287-4-3-126. Hered Cancer Clin Pract. 2006. PMID: 20223016 Free PMC article.

Discrepancy between initial high expression of interest in clinical cancer genetic testing and actual low uptake in an Asian population.

Chieng WS, Lee SC. Chieng WS, et al. Genet Test Mol Biomarkers. 2012 Jul;16(7):785-93. doi: 10.1089/gtmb.2011.0268. Epub 2012 Apr 26. Genet Test Mol Biomarkers. 2012. PMID: 22536849

Non-directive genetic counselling - respect for autonomy or unprofessional practice?

Chieng WS, Chan N, Lee SC. Chieng WS, et al. Ann Acad Med Singap. 2011 Jan;40(1):36-42. Ann Acad Med Singap. 2011. PMID: 21369631 Free article. Review.

Detection of promoter hypermethylation in serum samples of cancer patients by methylation-specific polymerase chain reaction for tumour suppressor genes including RUNX3.

Tan SH, Ida H, Lau QC, Goh BC, Chieng WS, Loh M, Ito Y. Tan SH, et al. Among authors: chieng ws. Oncol Rep. 2007 Nov;18(5):1225-30. Oncol Rep. 2007. PMID: 17914577

Inadequate family history assessment by oncologists is an important physician barrier to referral for hereditary breast cancer evaluation.

Ow SG, Yong YF, Chieng WS, Phyu PS, Lee SC. Ow SG, et al. Among authors: chieng ws. Clin Oncol (R Coll Radiol). 2014 Mar;26(3):174-5. doi: 10.1016/j.clon.2013.11.029. Epub 2014 Jan 4. Clin Oncol (R Coll Radiol). 2014. PMID: 24393786 No abstract available.

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