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Showing results 238 to 257 of 472 < previous next >

Title	Author(s)	Issue Date	Views
Impact of cytogenetic abnormality on the outcome of acute lymphoblastic leukaemia (ALL) in Chinese children Proceeding/Conference:Medical and Pediatric Oncology	Lee, ACW Chan, LC Chan, GCF Lau, YL	1994	104
Immunomodulators in Serious Pediatric Infections Proceeding/Conference:Annual Convention of the Pediatric Infectious Disease Society	Lau, YL	1994	96
Immunodeficiency and Childhood Malignancy Proceeding/Conference:HKICC / RPS 2000	Chan, GCF Lee, TL Ha, SY Lau, YL	2000
Immune responses of human respiratory epithelia cells to human metapneumovirus and respiratory syncytial virus Proceeding/Conference:International Congress of Immunology, IMMUNORIO 2007	Yip, MS Law, HKW Tu, W Lau, YL	2007	102
IL-6 Mediates the Inhibitory Effect of IGF-1 on PHA-Induced Apoptosis in Cord Blood T Cells Proceeding/Conference:International Congress of Pediatrics	Law, HKW Lau, YL	2001	88
IL-12p40 Homozygous ASN226 Genotype may be Protective Against Tuberculosis in Chinese Proceeding/Conference:Research Postgraduate Symposium, RPS 2002	Tso, HW Chiang, AKS Cheng, SKF Ip, EWK Tam, CM Lau, YL	2002	97
IFN-Gamma Microsatellite Region and Tuberculosis Proceeding/Conference:International Congress on Infectious Diseases	Cheng, FSK Tam, CM Lau, YL	2002	100
Identifying causal mutations for Primary Immunodeficiencies in Southeast Asian region using whole exome sequencing Proceeding/Conference:ICHG / ASHG 2011	Yang, J Yang, W Lee, PPW Zeng, S Zhang, L Sham, PC Lau, YL	2011	132
Identify a Novel CYBB Gene Mutation in a Chinese Boy with X-Linked Chronic Granulomer Disease and Its Carriers Proceeding/Conference:Hong Kong Journal of Paediatrics	Jiang, LP Mak, HS Wang, LJ Chan, KW Fang, P Luo, XJ Lau, YL Yang, XQ	2004
Identify a Novel Btk Splice Site Mutation in a Chinese Boy with XLA Proceeding/Conference:Hong Kong Journal of Paediatrics	Fang, P Jiang, LP Wang, JJ Wang, LJ Lau, YL Toshio, M Yang, XQ	2004	62
Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016	52
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, KC Ying, D Mak, CCY Chen, XY Xu, W Yeung, KS Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Lau, YL Lee, SL Chung, BHY	2016	30
Identification of 7 novel transforming growth factor β receptor 2 mutations in Chinese patients with marfan syndrome Proceeding/Conference:Pediatrics	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2008
Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007	106
Identification of 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC) Proceeding/Conference:International Congress of Pediatrics, IPA 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007
Identification of 25 novel and 2 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic: a missed burden in the transition care in Hong Kong Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Chung, B Chow, P Liu, A Lee, P Chan, K Tang, M Lau, E Cheung, YF Chau, KT Lau, YL	2013	82
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care Proceeding/Conference:European Journal of Human Genetics	Chung, B Chow, P Liu, A Lee, P Wong, V Chan, K Tang, M Lun, KS Lau, ETK Cheung, YF Chau, KT Lau, YL	2013	69
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:Annual Congress of the Asian Society for Pediatric Research, ASPR 2006	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006	114
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HUGO / HUGO-AP 2006	Lun, KS Lam, STS Tong, TMF Chung, BHY Li, YH Chan, HC Or, SF Lau, YL	2006	101

Showing results 238 to 257 of 472 < previous next >