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127 results

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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: tang mh, tang wf. 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
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: tang mh, tang wf. PLoS One. 2014 Oct 15;9(10):e109629. doi: 10.1371/journal.pone.0109629. eCollection 2014. PLoS One. 2014. PMID: 25333781 Free PMC article.
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: tang mh, tang wf. 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.
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.
Mak ASL, Chiu ATG, Leung GKC, Mak CCY, Chu YWY, Mok GTK, Tang WF, Chan KYK, Tang MHY, Lau Yim ET, So KW, Tao VQ, Fung CW, Wong VCN, Uddin M, Lee SL, Marshall CR, Scherer SW, Kan ASY, Chung BHY. Mak ASL, et al. Among authors: tang mhy, tang wf. Mol Autism. 2017 Jun 26;8:31. doi: 10.1186/s13229-017-0136-x. eCollection 2017. Mol Autism. 2017. PMID: 28670437 Free PMC article.
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
Siu WK, Lam CW, Mak CM, Lau ET, Tang MH, Tang WF, Poon-Mak RS, Lee CC, Hung SF, Leung PW, Kwong KL, Yau EK, Ng GS, Fong NC, Chan KY. Siu WK, et al. Among authors: tang mh, tang wf. Clin Transl Med. 2016 Dec;5(1):18. doi: 10.1186/s40169-016-0098-1. Epub 2016 May 16. Clin Transl Med. 2016. PMID: 27271878 Free PMC article.
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis.
Gill H, Ip HW, Yim R, Tang WF, Pang HH, Lee P, Leung GMK, Li J, Tang K, So JCC, Leung RYY, Li J, Panagioutou G, Lam CCK, Kwong YL. Gill H, et al. Among authors: tang k, tang wf. Ann Hematol. 2019 Apr;98(4):869-879. doi: 10.1007/s00277-018-3563-7. Epub 2018 Dec 4. Ann Hematol. 2019. PMID: 30515541 Clinical Trial.
127 results