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Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.
NPJ Genom Med. 2022 Mar 21;7(1):23. doi: 10.1038/s41525-022-00287-z.
NPJ Genom Med. 2022.
PMID: 35314707
Free PMC article.
Invasive cerebral phaeohyphomycosis in a Chinese boy with CARD9 deficiency and showing unique radiological features, managed with surgical excision and antifungal treatment.
Lai SHY, Duque JSR, Chung BH, Chung TW, Leung D, Ho RS, Lee R, Poon RWS, Chua GT, Cheong KN, Chui MMC, Lee M, Tam S, Him AHC, Cheng KF, Ho WW, Yuen KY, Lee P, Lau YL.
Lai SHY, et al. Among authors: chui mmc.
Int J Infect Dis. 2021 Jun;107:59-61. doi: 10.1016/j.ijid.2021.04.052. Epub 2021 Apr 16.
Int J Infect Dis. 2021.
PMID: 33872781
Free article.
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Functional Evaluation and Genetic Landscape of Children and Young Adults Referred for Assessment of Bronchiectasis.
Chau JFT, Lee M, Chui MMC, Yu MHC, Fung JLF, Mak CCY, Chau CS, Siu KK, Hung J, Yeung KS, Kwong AKY, O'Callaghan C, Lau YL, Lee CD, Chung BH, Lee SL.
Chau JFT, et al. Among authors: chui mmc.
Front Genet. 2022 Aug 8;13:933381. doi: 10.3389/fgene.2022.933381. eCollection 2022.
Front Genet. 2022.
PMID: 36003331
Free PMC article.
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Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.
Lai THT, Au LKS, Lau YTE, Lo HM, Chan KYK, Cheung KW, Ma TWL, Leung WC, Kong CW, Shu W, So PL, Kwong AKY, Mak CCY, Lee M, Chui MMC, Chung BHY, Kan ASY.
Lai THT, et al. Among authors: chui mmc.
Healthcare (Basel). 2022 Dec 13;10(12):2521. doi: 10.3390/healthcare10122521.
Healthcare (Basel). 2022.
PMID: 36554045
Free PMC article.
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Whole genome sequencing in paediatric channelopathy and cardiomyopathy.
Kwok SY, Kwong AKY, Shi JZ, Shih CFY, Lee M, Mak CCY, Chui M, Tsao S, Chung BHY.
Kwok SY, et al.
Front Cardiovasc Med. 2024 Mar 20;11:1335527. doi: 10.3389/fcvm.2024.1335527. eCollection 2024.
Front Cardiovasc Med. 2024.
PMID: 38586174
Free PMC article.
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Evaluating High-Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses.
Chui MMC, Mak CCY, Yu MHC, Wong SYY, Lun KS, Yung TC, Kwong AKY, Chow PC, Chung BHY.
Chui MMC, et al.
J Am Heart Assoc. 2023 Feb 21;12(4):e028226. doi: 10.1161/JAHA.122.028226. Epub 2023 Feb 15.
J Am Heart Assoc. 2023.
PMID: 36789878
Free PMC article.
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Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept.
Lee M, Kwong AKY, Chui MMC, Chau JFT, Mak CCY, Au SLK, Lo HM, Chan KYK, Yépez VA, Gagneur J, Kan ASY, Chung BHY.
Lee M, et al. Among authors: chui mmc.
NPJ Genom Med. 2022 Dec 28;7(1):74. doi: 10.1038/s41525-022-00347-4.
NPJ Genom Med. 2022.
PMID: 36577754
Free PMC article.
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