Results 1 to 12 of 12
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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, YL201076
Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypesChung, BHY; Lam, STS; Tong, TMF; Li, SYH; Lun, KS; Chan, DHC; Fok, SFS; Or, JSF; Smith, DK; Yang, W; Lau, YL2009125
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
Susceptibility to mycobacterial infections in children with x-linked chronic granulomatous disease: A review of 17 patients living in a region endemic for tuberculosisLee, PPW; Chan, KW; Jiang, L; Chen, T; Li, C; Lee, TL; Mak, PHS; Fok, SFS; Yang, X; Lau, YL2008157
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
The association of RANTES polymorphism with severe acute respiratory syndrome in Hong Kong and Beijing ChineseNg, MW; Zhou, G; Chong, WP; Lee, LWY; Law, HKW; Zhang, H; Wong, WHS; Fok, SFS; Zhai, Y; Yung, RWH; Chow, EY; Au, KL; Chan, EYT; Lim, W; Peiris, JSM; He, F; Lau, YL2007164
Resource of primary immunodeficiency diseases: genetic diagnosis in Hong KongChan, KW; Lee, TL; Jiang, L; Chen, TX; Lee, BW; Wang, X; Liew, WK; Li, G; Tan, AM; Noh, LM; Lim, DLC; Fok, SFS; Mak, HS; Lee, PPW; Yang, X; Lau, YL2007127
Clinical Characteristics and gp91phox Gene Mutations in Seventeen Chinese Children with X-linked Chronic Granulomatous DiseaseLee, PPW; Chan, KW; Lee, TL; Jiang, L; Mak, HS; Fok, SFS; Hui, YF; Li, C; Yang, X; Lau, YL2006102
Identification of Bruton tyrosine kinase mutations in 12 Chinese patients with X-linked agammaglobulinaemia by long PCR-direct sequencingChan, KW; Chen, T; Jiang, L; Fok, SFS; Lee, TL; Lee, BW; Yang, X; Lau, YL2006127
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
Modulating effects of mannose binding lectin genotype on arterial stiffness in children after Kawasaki diseaseCheung, YF; Ho, MHK; Ip, WK; Fok, SFS; Yung, TC; Lau, YL2004114
Mannose-binding lectin and Kawasaki disease in Southern Chinese childrenHo, MHK; Ip, EWK; Cheung, YF; Yung, TC; Cheng, VYW; Fok, SFS; Wong, WHS; Lau, YL200392
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