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Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs.
Chung CCY, Leung GKC, Mak CCY, Fung JLF, Lee M, Pei SLC, Yu MHC, Hui VCC, Chan JCK, Chau JFT, Chan MCY, Tsang MHY, Wong WHS, Tung JYL, Lun KS, Ng YK, Fung CW, Wong MSC, Wong RMS, Lau YL, Chan GCF, Lee SL, Yeung KS, Chung BHY. Chung CCY, et al. Among authors: leung gkc. Lancet Reg Health West Pac. 2020 Jul 24;1:100001. doi: 10.1016/j.lanwpc.2020.100001. eCollection 2020 Aug. Lancet Reg Health West Pac. 2020. PMID: 34327338 Free PMC article.
Diagnostic value of whole-exome sequencing in Chinese pediatric-onset neuromuscular patients.
Tsang MHY, Chiu ATG, Kwong BMH, Liang R, Yu MHC, Yeung KS, Ho WHL, Mak CCY, Leung GKC, Pei SLC, Fung JLF, Wong VCN, Muntoni F, Chung BHY, Chan SHS. Tsang MHY, et al. Among authors: leung gkc. Mol Genet Genomic Med. 2020 May;8(5):e1205. doi: 10.1002/mgg3.1205. Epub 2020 Mar 10. Mol Genet Genomic Med. 2020. PMID: 32154989 Free PMC article.
Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong.
Yu KPT, Luk HM, Leung GKC, Mak CCY, Cheng SSW, Hau EWL, Chan DKH, Lam STS, Tong TMF, Chung BHY, Lo IFM. Yu KPT, et al. Among authors: leung gkc. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):208-217. doi: 10.1002/ajmg.c.31692. Epub 2019 Mar 21. Am J Med Genet C Semin Med Genet. 2019. PMID: 30896080
22 results