Choy KW - Search Results

1

Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.

So PL, Hui ASY, Ma TWL, Shu W, Hui APW, Kong CW, Lo TK, Kan ANC, Kan EYL, Chong SC, Chung BHY, Luk HM, Choy KW, Kan ASY, Leung WC. So PL, et al. Among authors: choy kw. Genes (Basel). 2022 Nov 10;13(11):2088. doi: 10.3390/genes13112088. Genes (Basel). 2022. PMID: 36360323 Free PMC article.

2

Molecular genetics in fetal neurology.

Huang J, Wah IY, Pooh RK, Choy KW. Huang J, et al. Among authors: choy kw. Semin Fetal Neonatal Med. 2012 Dec;17(6):341-6. doi: 10.1016/j.siny.2012.07.007. Epub 2012 Aug 19. Semin Fetal Neonatal Med. 2012. PMID: 22909903 Review.

3

Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service.

Lau TK, Jiang FM, Stevenson RJ, Lo TK, Chan LW, Chan MK, Lo PS, Wang W, Zhang HY, Chen F, Choy KW. Lau TK, et al. Among authors: choy kw. Prenat Diagn. 2013 Jun;33(6):602-8. doi: 10.1002/pd.4076. Epub 2013 Apr 2. Prenat Diagn. 2013. PMID: 23553438

4

Noninvasive prenatal molecular karyotyping from maternal plasma.

Yu SC, Jiang P, Choy KW, Chan KC, Won HS, Leung WC, Lau ET, Tang MH, Leung TY, Lo YM, Chiu RW. Yu SC, et al. Among authors: choy kw. PLoS One. 2013 Apr 17;8(4):e60968. doi: 10.1371/journal.pone.0060968. Print 2013. PLoS One. 2013. PMID: 23613765 Free PMC article.

5

Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort.

Chong WW, Lo IF, Lam ST, Wang CC, Luk HM, Leung TY, Choy KW. Chong WW, et al. Among authors: choy kw. Mol Cytogenet. 2014 May 23;7:34. doi: 10.1186/1755-8166-7-34. eCollection 2014. Mol Cytogenet. 2014. PMID: 24926319 Free PMC article.

6

Combined Count- and Size-Based Analysis of Maternal Plasma DNA for Noninvasive Prenatal Detection of Fetal Subchromosomal Aberrations Facilitates Elucidation of the Fetal and/or Maternal Origin of the Aberrations.

Yu SC, Jiang P, Chan KC, Faas BH, Choy KW, Leung WC, Leung TY, Lo YM, Chiu RW. Yu SC, et al. Among authors: choy kw. Clin Chem. 2017 Feb;63(2):495-502. doi: 10.1373/clinchem.2016.254813. Epub 2016 Dec 14. Clin Chem. 2017. PMID: 27974386

7

Identification of a PTEN mutation with reduced protein stability, phosphatase activity, and nuclear localization in Hong Kong patients with autistic features, neurodevelopmental delays, and macrocephaly.

Wong CW, Or PMY, Wang Y, Li L, Li J, Yan M, Cao Y, Luk HM, Tong TMF, Leslie NR, Lo IF, Choy KW, Chan AML. Wong CW, et al. Among authors: choy kw. Autism Res. 2018 Aug;11(8):1098-1109. doi: 10.1002/aur.1950. Epub 2018 Apr 2. Autism Res. 2018. PMID: 29608813 Free PMC article.

8

Low-pass genome sequencing: a validated method in clinical cytogenetics.

Chau MHK, Wang H, Lai Y, Zhang Y, Xu F, Tang Y, Wang Y, Chen Z, Leung TY, Chung JPW, Kwok YK, Chong SC, Choy KW, Zhu Y, Xiong L, Wei W, Dong Z. Chau MHK, et al. Among authors: choy kw. Hum Genet. 2020 Nov;139(11):1403-1415. doi: 10.1007/s00439-020-02185-9. Epub 2020 May 25. Hum Genet. 2020. PMID: 32451733

9

The Pregnancy Outcome of Mosaic Embryo Transfer: A Prospective Multicenter Study and Meta-Analysis.

Zhang YX, Chen JJ, Nabu S, Yeung QSY, Li Y, Tan JH, Suksalak W, Chanchamroen S, Quangkananurug W, Wong PS, Chung JPW, Choy KW. Zhang YX, et al. Among authors: choy kw. Genes (Basel). 2020 Aug 21;11(9):973. doi: 10.3390/genes11090973. Genes (Basel). 2020. PMID: 32825792 Free PMC article.

10

Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review.

Zhu X, Lam DYM, Chau MHK, Xue S, Dai P, Zhao G, Cao Y, Cheung SWH, Kwok YKY, Choy KW, Kong X, Leung TY. Zhu X, et al. Among authors: choy kw. Genes (Basel). 2020 Dec 24;12(1):11. doi: 10.3390/genes12010011. Genes (Basel). 2020. PMID: 33374124 Free PMC article. Review.

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