Results 1 to 16 of 16
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TypeTitleAuthor(s)YearViews
Unique Pattern of Infections in Chronic Granulomatous Disease – The Asian ExperienceLee, PPW; He, JX; Chan, KW; Yang, W; Jiang, LP; Liew, WK; Chen, TX; Ho, MHK; Lee, TL; Lau, YL201332
 
Molecular diagnosis of severe combined immunodeficiency - Identification of IL2RG, JAK3, IL7R, DCLRE1C, RAG1, and RAG2 mutations in a cohort of Chinese and Southeast Asian childrenLee, PPW; Chan, KW; Chen, TX; Jiang, LP; Wang, XC; Zeng, HS; Chen, XY; Liew, WK; Chen, J; Chu, KM; Chan, LL; Shek, L; Lee, ACW; Yu, HH; Li, Q; Xu, CG; SultanUgdoracion, G; Latiff, ZA; Latiff, AHA; Jirapongsananuruk, O; Ho, MHK; Lee, TL; Yang, XQ; Lau, YL2011148
 
Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemiaLee, PPW; Chen, TX; Jiang, LP; Chan, KW; Yang, W; Lee, BW; Chiang, WC; Chen, XY; Fok, SFS; Lee, TL; Ho, MHK; Yang, XQ; Lau, YL201077
 
Molecular diagnosis of severe combined immunodeficiency - Identification of IL2RG, JAK3, IL7R, DCLRE1C and RAG2 mutations in a cohort of Chinese and Southeast Asian childrenLee, PPW; Chan, KW; Chen, TX; Jiang, LP; Wang, XC; Zeng, HS; Chen, XY; Lee, BW; Shek, L; Liew, WK; Lee, ACW; Yu, HH; Latiff, ZA; Ho, MHK; Lee, TL; Lau, YL2010224
 
Clinical and molecular characteristics of 35 chinese children with wiskott-aldrich syndromeLee, PPW; Chen, TX; Jiang, LP; Chen, J; Chan, KW; Lee, TL; Ho, MHK; Nong, SH; Yang, Y; Fang, YJ; Li, Q; Wang, XC; Yang, XQ; Lau, YL2009185
 
Molecular Analysis of 12 Chinese patients with X-linked Hyper-IgM syndromeLee, PPW; Ho, MHK; Chan, KW; Chen, TX; Jiang, LP; Lee, BW; Liew, WK; Tan, AM; Lam, J; Lee, TL; Yu, HH; Huang, L; Yang, XQ; Lau, YL2009183
 
Inherited Defects in Interleukin-12/Interferon-gamma Pathway in Patients with Unusual Mycobacterial InfectionsLee, PPW; Chan, KW; Chen, TX; Jiang, LP; Wang, XC; Lee, JT; Lung, DC; Chiang, WC; Yi, ZW; Amir, HL; Lokman, MN; Lau, YL2009182
 
Genotype-Phenotype Correlation Study in 62 Patients with X-Linked Agammaglobulinemia Human Immunology and ImmunodeficienciesLee, PPW; Chen, TX; Jiang, LP; Chan, KW; Yang, W; Lee, BW; Chiang, WC; Chen, XY; Fok, SFS; Lee, TL; Ho, MHK; Yang, XQ; Lau, YL2009182
 
Clinical and Molecular Characteristics of 32 Chinese Children with Wiskott-Aldrich SyndromeLee, PPW; Chen, TX; Jiang, LP; Chen, J; Chan, KW; Lee, TL; Ho, MHK; Nong, SH; Yang, Y; Fang, YJ; Li, Q; Yang, XQ; Lau, YL2009200
 
Severe mycobacterial infections in two pairs of Chinese siblings with interleukin-12 receptor β1 deficiencyLee, PPW; Jiang, LP; Wang, XC; Chan, KW; Tu, WW; Lau, YL2008100
 
Clinical, Immunological and Molecular Characteristics of 67 Chinese Patients with X-Linked AgammaglobulinemiaLee, PPW; Chen, TX; Yang, W; Jiang, LP; Chan, KW; Fok, SFS; Lee, TL; Lau, YL2008131
 
Identify a Novel Btk Splice Site Mutation in a Chinese Boy with XLAFang, P; Jiang, LP; Wang, JJ; Wang, LJ; Lau, YL; Toshio, M; Yang, XQ200489
 
A Novel Btk Gene Mutation in a Chinese Boy with XLA and Its CarriersJiang, LP; Fok, SFS; Wang, LJ; Chan, KW; Wang, M; Liu, EM; Li, X; Deng, B; Yang, XQ; Lau, YL; Toshio, M200486
 
Two Novel ITGB2 Gene Mutations in a Chinese Boy with Leucocyte Adhesion Deficiency Type 1Jiang, LP; Chan, KW; Liu, EM; Law, HKW; Li, X; Deng, B; Wang, LJ; Yang, XQ; Lau, YL2004112
 
Identify a Novel CYBB Gene Mutation in a Chinese Boy with X-Linked Chronic Granulomer Disease and Its CarriersJiang, LP; Mak, HS; Wang, LJ; Chan, KW; Fang, P; Luo, XJ; Lau, YL; Yang, XQ200496
 
Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndromeJiang, LP; Xu, YH; Yang, XQ; Liu, EM; Wang, LJ; Lau, YL; Chan, KW200377
 
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