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Erratum to: recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history.
Kang PC, Phuah SY, Sivanandan K, Kang IN, Thirthagiri E, Liu JJ, Hassan N, Yoon SY, Thong MK, Hui M, Hartman M, Yip CH, Taib NA, Teo SH. Kang PC, et al. Among authors: kang in. Breast Cancer Res Treat. 2015 Apr;150(3):699-700. doi: 10.1007/s10549-015-3360-0. Breast Cancer Res Treat. 2015. PMID: 25833212 No abstract available.
Recurrent mutation testing of BRCA1 and BRCA2 in Asian breast cancer patients identify carriers in those with presumed low risk by family history.
Kang PC, Phuah SY, Sivanandan K, Kang IN, Thirthagiri E, Liu JJ, Hassan N, Yoon SY, Thong MK, Hui M, Hartman M, Yip CH, Mohd Taib NA, Teo SH. Kang PC, et al. Among authors: kang in. Breast Cancer Res Treat. 2014 Apr;144(3):635-42. doi: 10.1007/s10549-014-2894-x. Epub 2014 Mar 1. Breast Cancer Res Treat. 2014. PMID: 24578176
Comparable frequency of BRCA1, BRCA2 and TP53 germline mutations in a multi-ethnic Asian cohort suggests TP53 screening should be offered together with BRCA1/2 screening to early-onset breast cancer patients.
Lee DS, Yoon SY, Looi LM, Kang P, Kang IN, Sivanandan K, Ariffin H, Thong MK, Chin KF, Mohd Taib NA, Yip CH, Teo SH. Lee DS, et al. Breast Cancer Res. 2012 Apr 16;14(2):R66. doi: 10.1186/bcr3172. Breast Cancer Res. 2012. PMID: 22507745 Free PMC article.
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