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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. Among authors: chan ky. 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
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. Among authors: chan ss, chan ky. 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.
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. Among authors: chan ky. PLoS One. 2014 Oct 15;9(10):e109629. doi: 10.1371/journal.pone.0109629. eCollection 2014. PLoS One. 2014. PMID: 25333781 Free PMC article.
829 results