| Title | Author(s) | Year | View Count |
 | An 11-bp deletion in exon 10 (c1295del11) of WASP responsible for Wiskott-Aldrich Syndrome | Chan, SY; Hui, YF; Lau, YL | 1999 | 175 |
 | 15 years' review of neuroblastoma from a single institution | Chan, KL; Saing, H; Tam, PKH; Cheung, N; Chan, GCF; Ha, SY; Lau, YL | 1996 | 233 |
| 17p13.3 class I microduplication in a newborn with microcephaly, aortic stenosis and dysmorphic facial features | Ho, A; Liu, A; Lun, KS; Tam, T; Chan, K; Lau, E; Tang, M; Tan, T; Chung, B | 2011 | 152 |
| 2001 Keystone Symposium: Decreased yield, phenotypic expression and function of immature monocyte-derived dendritic cells in cord blood | Liu, EM; Tu, WW; Law, HKW; Lau, YL | 2001 | 161 |
| 2009年自閉症 | Wong, VCN | 2009 | 183 |
 | The 23-valent polysaccharide pneumococcal vaccination is not useful in BMT patients at risk of pneumococcal bacteremic sepsis | Leung, AYH; Lie, AKW; Kwong, YL; Yuen, KY; Au, WY; Wong, KK; Kwok, JSY; Lee, TL; Cheng, VCC; Liang, RHS | 2001 | 479 |
| 2nd Health Education Booklet with Metro Daily, LKS Faculty of Medicine, HKU | Chan, GCF | 2010 | 177 |
| 2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial features | Chung, BH; Stavropoulos, J; Marshall, CR; Weksberg, R; Scherer, SW; Yoon, G | 2011 | 340 |
| A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression | Farrell, JJ; Sherva, RM; Chen, ZY; Luo, HY; Chu, BF; Ha, SY; Li, CK; Lee, ACW; Li, RCH; Li, CK; Yuen, HL; So, JCC; Ma, ESK; Chan, LC; Chan, V; Sebastiani, P; Farrer, LA; Baldwin, CT; Steinberg, MH; Chui, DHK | 2011 | 157 |
| A 3D collagen microsphere culture system for GDNF-secreting HEK293 cells with enhanced protein productivity | Wong, HL; Wang, MX; Cheung, PT; Yao, KM; Chan, BP | 2007 | 258 |
| A 48-month follow-up of a randomized controlled trial on a stage-matched smoking cessation intervention among cardiac patients | Chan, SSC; Leung, YP; Leung, GM; Wong, V; Lam, TH | 2009 | 323 |
| 6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystonia | Fung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN | 2005 | 112 |
| 6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patients | Fung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN | 2006 | 121 |
| An 8-year-old girl with urticaria since birth | Lee, TL; Chan, KW; Lau, YL | 2006 | 119 |
| An 8-year-old Girl with Urticaria Since Birth | Lee, TL; Chan, KW; Hon, C; Lau, YL | 2004 | 110 |
| A cohort study on prematurity as an indicator of autistic symptom severity | Chung, Weiyen.; 钟慧元. | 2012 | 162 |
| A pilot study on potential involvement of epigenetic regulations secondary to perturbed intrauterine environment | Lam, Shih-en.; 林詩恩. | 2008 | 309 |
| A role of TSPYL2, a novel nucleosome assembly protein, in transcriptional regulation | Wong, Hiu-ting.; 王曉婷. | 2009 | 310 |
| A transgenic mouse model to study the role of epidermal growthfactor (EGF) in hair and skin development | Mak, King-lun, Kingston.; 麥經綸 | 2002 | 352 |
| ABC of Apoptosis in Neurological Disorders | Cheung, PT | 2003 | 79 |
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