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Results 1 to 20 of 3309
Page 1 of 166  Next >
TypeTitleAuthor(s)YearViews
An 11-bp deletion in exon 10 (c1295del11) of WASP responsible for Wiskott-Aldrich SyndromeChan, SY; Hui, YF; Lau, YL1999190
 
15 years' review of neuroblastoma from a single institutionChan, KL; Saing, H; Tam, PKH; Cheung, N; Chan, GCF; Ha, SY; Lau, YL1996248
 
17p13.3 class I microduplication in a newborn with microcephaly, aortic stenosis and dysmorphic facial featuresHo, A; Liu, A; Lun, KS; Tam, T; Chan, K; Lau, E; Tang, M; Tan, T; Chung, B2011164
 
2001 Keystone Symposium: Decreased yield, phenotypic expression and function of immature monocyte-derived dendritic cells in cord bloodLiu, EM; Tu, WW; Law, HKW; Lau, YL2001193
 
2009年自閉症Wong, VCN2009177
 
22q11.2 deletion syndrome in adult Chinese patient with conotruncal anomalies: Dysmorphisms, clinical features and under-diagnosisLiu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, KY; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201336
 
22q11.2 deletion syndrome in adult Chinese patients with conotruncal anomalies: dysmorphisms, clinical features and under-diagnosisLiu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, YK; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201333
 
The 23-valent polysaccharide pneumococcal vaccination is not useful in BMT patients at risk of pneumococcal bacteremic sepsisLeung, AYH; Lie, AKW; Kwong, YL; Yuen, KY; Au, WY; Wong, KK; Kwok, JSY; Lee, TL; Cheng, VCC; Liang, RHS2001459
 
2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial featuresChung, BH; Stavropoulos, J; Marshall, CR; Weksberg, R; Scherer, SW; Yoon, G2011329
 
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionFarrell, 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, DHK2011184
 
A 3D collagen microsphere culture system for GDNF-secreting HEK293 cells with enhanced protein productivityWong, HL; Wang, MX; Cheung, PT; Yao, KM; Chan, BP2007273
 
A 48-month follow-up of a randomized controlled trial on a stage-matched smoking cessation intervention among cardiac patientsChan, SSC; Leung, YP; Leung, GM; Wong, V; Lam, TH2009321
 
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystoniaFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2005125
 
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patientsFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2006116
 
An 8-year-old girl with urticaria since birthLee, TL; Chan, KW; Lau, YL2006127
 
An 8-year-old Girl with Urticaria Since BirthLee, TL; Chan, KW; Hon, C; Lau, YL2004149
 
A cohort study on prematurity as an indicator of autistic symptom severityChung, Weiyen.; 钟慧元.2012150
 
A pilot study on potential involvement of epigenetic regulations secondary to perturbed intrauterine environmentLam, Shih-en.; 林詩恩.2008227
 
A role of TSPYL2, a novel nucleosome assembly protein, in transcriptional regulationWong, Hiu-ting.; 王曉婷.2009221
 
A transgenic mouse model to study the role of epidermal growthfactor (EGF) in hair and skin developmentMak, King-lun, Kingston.; 麥經綸2002315
 
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