Results 1 to 5 of 5
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TypeTitleAuthor(s)YearViews
Clinical Characteristics and gp91phox Gene Mutations in Seventeen Chinese Children with X-linked Chronic Granulomatous Disease
Proceedings/Conference:
2nd Congress of Asian Society for Pediatric Research (ASPR), Yokohama, Japan, 8-10 December 2006
Lee, PPW; Chan, KW; Lee, TL; Jiang, L; Mak, HS; Fok, SFS; Hui, YF; Li, C; Yang, X; Lau, YL2006137
 
Detection of genetic defect of childhood acute leukaemia by reverse transcriptase polymerase chain reaction (RT-PCR): An essential component for risk directed therapy approach
Proceedings/Conference:
The Hong Kong Paediatric Society, 35th Anniversary Scientific Meeting, QEH, September 6, 1997
Chan, GCF; Chan, SY; Lee, DCW; Hui, YF; Ma, ESK; Ha, SY; Lee, ACW; Ling, SC; Li, CK; Luk, CW; Chiu, DCK; Chan, LC; Lau, YL1997101
 
Mutation studies of Chinese patients with Wiskott-Aldrich Syndrome
Proceedings/Conference:
The Hong Kong Paediatric Society, 35th Anniversary Scientific Meeting, QEH, September 6, 1997
Hui, YF; Chan, SY; Lau, YL199784
 
Expression of gp91phox-like-protein in patients with XO-CGD
Proceedings/Conference:
Journal of Paediatrics and Child Health
Publisher:
Blackwell Publishing Asia.
Hui, YF; Chan, SY; Lau, YL199797
 
Mycobacterium tuberculosis is a major pathogen in patients with chronic granulomatous disease
Proceedings/Conference:
Chinese Paediatric Forum, November 15-17, 1996
Lau, YL; Yuen, KY; Ha, SY; Chan, CF; Hui, YF1996113
 
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