Chan KYK - Search Results

1

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).

Leung GKC, Mak CCY, Fung JLF, Wong WHS, Tsang MHY, Yu MHC, Pei SLC, Yeung KS, Mok GTK, Lee CP, Hui APW, Tang MHY, Chan KYK, Liu APY, Yang W, Sham PC, Kan ASY, Chung BHY. Leung GKC, et al. Among authors: chan kyk. BMC Med Genomics. 2018 Oct 25;11(1):93. doi: 10.1186/s12920-018-0409-z. BMC Med Genomics. 2018. PMID: 30359267 Free PMC article.

2

A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - is cardiac assessment necessary for all patients with 17p13.3 microduplication?

Ho AC, Liu AP, Lun KS, Tang WF, Chan KY, Lau EY, Tang MH, Tan TY, Chung BH. Ho AC, et al. Eur J Med Genet. 2012 Dec;55(12):758-62. doi: 10.1016/j.ejmg.2012.09.011. Epub 2012 Oct 9. Eur J Med Genet. 2012. PMID: 23063769

3

Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: report and a review of literature.

Liu AP, Tang WF, Lau ET, Chan KY, Kan AS, Wong KY, Tso WW, Jalal K, Lee SL, Chau CS, Chung BH. Liu AP, et al. Am J Med Genet A. 2013 Jun;161A(6):1309-18. doi: 10.1002/ajmg.a.35909. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633107 Review.

4

A prenatal case of split-hand malformation associated with 17p13.3 triplication - a dilemma in genetic counseling.

Luk HM, Wong VC, Lo IF, Chan KY, Lau ET, Kan AS, Tang MH, Tang WF, She WM, Chu YW, Sin WK, Chung BH. Luk HM, et al. Eur J Med Genet. 2014 Feb;57(2-3):81-4. doi: 10.1016/j.ejmg.2013.12.005. Epub 2013 Dec 28. Eur J Med Genet. 2014. PMID: 24380768

5

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.

Kan AS, Lau ET, Tang WF, Chan SS, Ding SC, Chan KY, Lee CP, Hui PW, Chung BH, Leung KY, Ma T, Leung WC, Tang MH. Kan AS, et al. PLoS One. 2014 Feb 5;9(2):e87988. doi: 10.1371/journal.pone.0087988. eCollection 2014. PLoS One. 2014. PMID: 24505343 Free PMC article. Clinical Trial.

6

Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.

Liu AP, Chow PC, Lee PP, Mok GT, Tang WF, Lau ET, Lam ST, Chan KY, Kan AS, Chau AK, Cheung YF, Lau YL, Chung BH. Liu AP, et al. Eur J Med Genet. 2014 May-Jun;57(6):306-11. doi: 10.1016/j.ejmg.2014.03.014. Epub 2014 Apr 8. Eur J Med Genet. 2014. PMID: 24721633

7

Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.

Yeung KS, Chee YY, Luk HM, Kan AS, Tang MH, Lau ET, Shuen AY, Lo IF, Chan KY, Chung BH. Yeung KS, et al. Am J Med Genet A. 2014 Oct;164A(10):2521-8. doi: 10.1002/ajmg.a.36670. Epub 2014 Jul 16. Am J Med Genet A. 2014. PMID: 25044945

8

The clinical impact of chromosomal microarray on paediatric care in Hong Kong.

Tao VQ, Chan KY, Chu YW, Mok GT, Tan TY, Yang W, Lee SL, Tang WF, Tso WW, Lau ET, Kan AS, Tang MH, Lau YL, Chung BH. Tao VQ, et al. PLoS One. 2014 Oct 15;9(10):e109629. doi: 10.1371/journal.pone.0109629. eCollection 2014. PLoS One. 2014. PMID: 25333781 Free PMC article.

9

A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.

Au PK, Kan AS, Tang MH, Leung KY, Chan KY, Tang TW, Lau ET. Au PK, et al. Hemoglobin. 2016;40(1):66-9. doi: 10.3109/03630269.2015.1096283. Epub 2015 Nov 16. Hemoglobin. 2016. PMID: 26574185

10

Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome.

Kou KO, Poon CF, Kwok SL, Chan KY, Tang MH, Kan AS, Leung KY. Kou KO, et al. Hong Kong Med J. 2016 Jun;22(3):223-30. doi: 10.12809/hkmj154730. Epub 2016 May 6. Hong Kong Med J. 2016. PMID: 27149976 Free article.

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