Leung TY - Search Results

1

Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi-Center Cohort Study.

Li K, Wang H, Chau MHK, Dong Z, Cao Y, Zheng Y, Leung TY, Choy KW, Zhu Y. Li K, et al. Among authors: leung ty. Prenat Diagn. 2024 Nov;44(12):1451-1461. doi: 10.1002/pd.6674. Epub 2024 Oct 3. Prenat Diagn. 2024. PMID: 39363241

2

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. Among authors: leung ty. Prenat Diagn. 2020 Jul;40(8):1005-1012. doi: 10.1002/pd.5721. Epub 2020 May 17. Prenat Diagn. 2020. PMID: 32350887

3

Noninvasive prenatal sequencing for multiple Mendelian monogenic disorders among fetuses with skeletal dysplasia or increased nuchal translucency.

Yan H, Zhu X, Chen J, Cao Y, Kwok YKY, Chen Z, Leung TY, Chen M, Choy KW. Yan H, et al. Among authors: leung ty. Prenat Diagn. 2020 Oct;40(11):1459-1465. doi: 10.1002/pd.5792. Epub 2020 Aug 17. Prenat Diagn. 2020. PMID: 32668031 Clinical Trial.

4

Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects.

Cao Y, Chau MHK, Zheng Y, Zhao Y, Kwan AHW, Hui SYA, Lam YH, Tan TYT, Tse WT, Wong L, Leung TY, Dong Z, Choy KW. Cao Y, et al. Among authors: leung ty. Prenat Diagn. 2022 Jun;42(7):862-872. doi: 10.1002/pd.6151. Epub 2022 Apr 27. Prenat Diagn. 2022. PMID: 35441720

5

Chinese women's preferences for prenatal diagnostic procedure and their willingness to trade between procedures.

Chan YM, Sahota DS, Leung TY, Choy KW, Chan OK, Lau TK. Chan YM, et al. Among authors: leung ty. Prenat Diagn. 2009 Dec;29(13):1270-6. doi: 10.1002/pd.2394. Prenat Diagn. 2009. PMID: 19862769

6

The detection of mosaicism by prenatal BoBs™.

Cheng YK, Wong C, Wong HK, Leung KO, Kwok YK, Suen A, Wang CC, Leung TY, Choy KW. Cheng YK, et al. Among authors: leung ko, leung ty. Prenat Diagn. 2013 Jan;33(1):42-9. doi: 10.1002/pd.4006. Epub 2012 Nov 20. Prenat Diagn. 2013. PMID: 23168997

7

Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses.

Zhou Y, Huang J, Cheng YK, Leung TY, Pooh RK, Lo FM, Choy KW. Zhou Y, et al. Among authors: leung ty. Prenat Diagn. 2014 Mar;34(3):296-8. doi: 10.1002/pd.4292. Epub 2013 Dec 23. Prenat Diagn. 2014. PMID: 24375696 No abstract available.

8

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: leung ty. Mol Cytogenet. 2014 May 23;7:34. doi: 10.1186/1755-8166-7-34. eCollection 2014. Mol Cytogenet. 2014. PMID: 24926319 Free PMC article.

9

Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.

Cao Y, Li Z, Rosenfeld JA, Pursley AN, Patel A, Huang J, Wang H, Chen M, Sun X, Leung TY, Cheung SW, Choy KW. Cao Y, et al. Among authors: leung ty. Genet Med. 2016 Oct;18(10):1052-5. doi: 10.1038/gim.2015.216. Epub 2016 Feb 25. Genet Med. 2016. PMID: 26913922 Free article.

10

Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.

Kong GW, Cao Y, Huang J, Cheng KY, Pursley AN, Rosenfeld JA, Edwards JG, Chan YM, Cheung SW, Leung TY, Choy KW. Kong GW, et al. Among authors: leung ty. Prenat Diagn. 2016 Dec;36(13):1211-1216. doi: 10.1002/pd.4959. Epub 2016 Nov 29. Prenat Diagn. 2016. PMID: 27859473

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