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Efficient detection of copy-number variations using exome data: Batch- and sex-based analyses.
Hum Mutat. 2021 Jan;42(1):50-65. doi: 10.1002/humu.24129. Epub 2020 Nov 11.
Hum Mutat. 2021.
PMID: 33131168
Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures.
Nakashima M, Tohyama J, Nakagawa E, Watanabe Y, Siew CG, Kwong CS, Yamoto K, Hiraide T, Fukuda T, Kaname T, Nakabayashi K, Hata K, Ogata T, Saitsu H, Matsumoto N.
Nakashima M, et al. Among authors: siew cg.
J Hum Genet. 2019 Apr;64(4):313-322. doi: 10.1038/s10038-018-0559-z. Epub 2019 Jan 17.
J Hum Genet. 2019.
PMID: 30655572
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Genetic Testing for Cancer Risk: Is the Community Willing to Pay for It?
Aizuddin AN, Ramdzan AR, Syed Omar SA, Mahmud Z, Latiff ZA, Amat S, Teik KW, Siew CG, Rais H, Aljunid SM.
Aizuddin AN, et al. Among authors: siew cg.
Int J Environ Res Public Health. 2021 Aug 19;18(16):8752. doi: 10.3390/ijerph18168752.
Int J Environ Res Public Health. 2021.
PMID: 34444499
Free PMC article.
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Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.
Mohd Khalid MK, Yakob Y, Md Yasin R, Wee Teik K, Siew CG, Rahmat J, Ramasamy S, Alagaratnam J.
Mohd Khalid MK, et al. Among authors: siew cg.
Mol Vis. 2015 Oct 14;21:1185-90. eCollection 2015.
Mol Vis. 2015.
PMID: 26539030
Free PMC article.
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