Chau MHK - Search Results

1

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing.

Mitchell CO, Rivera-Cruz G, Chau MHK, Dong Z, Choy KW, Shen J, Amr S, Giersch ABS, Morton CC. Mitchell CO, et al. Among authors: chau mhk. Int J Neonatal Screen. 2022 May 27;8(2):36. doi: 10.3390/ijns8020036. Int J Neonatal Screen. 2022. PMID: 35735787 Free PMC article.

2

Chromosome copy number variants in fetuses with syndromic malformations.

Wang H, Chau MHK, Cao Y, Kwok KY, Choy KW. Wang H, et al. Among authors: chau mhk. Birth Defects Res. 2017 Jun 1;109(10):725-733. doi: 10.1002/bdr2.1054. Birth Defects Res. 2017. PMID: 28568742 Review.

3

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.

Chau MHK, Cao Y, Kwok YKY, Chan S, Chan YM, Wang H, Yang Z, Wong HK, Leung TY, Choy KW. Chau MHK, et al. Am J Obstet Gynecol. 2019 Nov;221(5):493.e1-493.e11. doi: 10.1016/j.ajog.2019.06.007. Epub 2019 Jun 14. Am J Obstet Gynecol. 2019. PMID: 31207233

4

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.

Wang H, Dong Z, Zhang R, Chau MHK, Yang Z, Tsang KYC, Wong HK, Gui B, Meng Z, Xiao K, Zhu X, Wang Y, Chen S, Leung TY, Cheung SW, Kwok YK, Morton CC, Zhu Y, Choy KW. Wang H, et al. Among authors: chau mhk. Genet Med. 2020 Mar;22(3):500-510. doi: 10.1038/s41436-019-0634-7. Epub 2019 Aug 26. Genet Med. 2020. PMID: 31447483 Free PMC article.

5

Reply.

Chau MHK, Sahota DS, Choy KW, Choy KW. Chau MHK, et al. Am J Obstet Gynecol. 2019 Dec;221(6):661-662. doi: 10.1016/j.ajog.2019.08.029. Epub 2019 Aug 27. Am J Obstet Gynecol. 2019. PMID: 31469991 No abstract available.

6

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.

Choy KW, Wang H, Shi M, Chen J, Yang Z, Zhang R, Yan H, Wang Y, Chen S, Chau MHK, Cao Y, Chan OYM, Kwok YK, Zhu Y, Chen M, Leung TY, Dong Z. Choy KW, et al. Among authors: chau mhk. Front Genet. 2019 Aug 16;10:761. doi: 10.3389/fgene.2019.00761. eCollection 2019. Front Genet. 2019. PMID: 31475041 Free PMC article.

7

The utility of genome-wide cell-free DNA screening in the prenatal diagnosis of Pallister-Killian syndrome.

Chau MHK, Lam DYM, Zhu X, Kwok YKY, Ting YH, Chan WP, Shi M, Cheung SWH, Lau TK, Ville Y, Leung TY, Choy KW. Chau MHK, et al. Prenat Diagn. 2020 Jul;40(8):1005-1012. doi: 10.1002/pd.5721. Epub 2020 May 17. Prenat Diagn. 2020. PMID: 32350887

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. 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

Deciphering the complexity of simple chromosomal insertions by genome sequencing.

Dong Z, Chau MHK, Zhang Y, Dai P, Zhu X, Leung TY, Kong X, Kwok YK, Stankiewicz P, Cheung SW, Choy KW. Dong Z, et al. Among authors: chau mhk. Hum Genet. 2021 Feb;140(2):361-380. doi: 10.1007/s00439-020-02210-x. Epub 2020 Jul 29. Hum Genet. 2021. PMID: 32728808

10

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.

Hui AS, Chau MHK, Chan YM, Cao Y, Kwan AH, Zhu X, Kwok YK, Chen Z, Lao TT, Choy KW, Leung TY. Hui AS, et al. Among authors: chau mhk. Acta Obstet Gynecol Scand. 2021 Feb;100(2):235-243. doi: 10.1111/aogs.14003. Epub 2020 Oct 15. Acta Obstet Gynecol Scand. 2021. PMID: 32981064 Free article.

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