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Silver-Russell syndrome in Hong Kong.
Luk HM, Yeung KS, Wong WL, Chung BH, Tong TM, Lo IF. Luk HM, et al. Among authors: chung bh. Hong Kong Med J. 2016 Dec;22(6):526-33. doi: 10.12809/hkmj154750. Epub 2016 Jul 29. Hong Kong Med J. 2016. PMID: 27468965 Free article.
Chronic benign neutropenia among Chinese children.
Chung BH, Chan GC, Lee T, Kwok JS, Chiang AK, Ho HK, Ha SY, Lau YL. Chung BH, et al. Hong Kong Med J. 2004 Aug;10(4):231-6. Hong Kong Med J. 2004. PMID: 15299167 Free article.
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: chung bh. PLoS One. 2014 Oct 15;9(10):e109629. doi: 10.1371/journal.pone.0109629. eCollection 2014. PLoS One. 2014. PMID: 25333781 Free PMC article.
NSD1 mutations generate a genome-wide DNA methylation signature.
Choufani S, Cytrynbaum C, Chung BH, Turinsky AL, Grafodatskaya D, Chen YA, Cohen AS, Dupuis L, Butcher DT, Siu MT, Luk HM, Lo IF, Lam ST, Caluseriu O, Stavropoulos DJ, Reardon W, Mendoza-Londono R, Brudno M, Gibson WT, Chitayat D, Weksberg R. Choufani S, et al. Among authors: chung bh. Nat Commun. 2015 Dec 22;6:10207. doi: 10.1038/ncomms10207. Nat Commun. 2015. PMID: 26690673 Free PMC article.
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis.
Leung GK, Ying D, Mak CC, Chen XY, Xu W, Yeung KS, Wong WL, Chu YW, Mok GT, Chau CS, McLuskey J, Ong WP, Leong HY, Chan KY, Yang W, Chen JH, Li AM, Sham PC, Lau YL, Chung BH, Lee SL. Leung GK, et al. Among authors: chung bh. Mol Genet Genomic Med. 2016 Nov 13;5(1):40-49. doi: 10.1002/mgg3.258. eCollection 2017 Jan. Mol Genet Genomic Med. 2016. PMID: 28116329 Free PMC article.
994 results