| Title | Author(s) | Year | View Count |
 | Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemia | Lee, PPW; Chen, TX; Jiang, LP; Chan, KW; Yang, W; Lee, BW; Chiang, WC; Chen, XY; Fok, SFS; Lee, TL; Ho, MHK; Yang, XQ; Lau, YL | 2010 | 54 |
 | Genotype-Phenotype Correlation Study in 62 Patients with X-Linked Agammaglobulinemia Human Immunology and Immunodeficiencies | Lee, PPW; Chen, TX; Jiang, LP; Chan, KW; Yang, W; Lee, BW; Chiang, WC; Chen, XY; Fok, SFS; Lee, TL; Ho, MHK; Yang, XQ; Lau, YL | 2009 | 184 |
| Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes | Chung, BHY; Lam, STS; Tong, TMF; Li, SYH; Lun, KS; Chan, DHC; Fok, SFS; Or, JSF; Smith, DK; Yang, W; Lau, YL | 2009 | 62 |
| Susceptibility to mycobacterial infections in children with x-linked chronic granulomatous disease: A review of 17 patients living in a region endemic for tuberculosis | Lee, PPW; Chan, KW; Jiang, L; Chen, T; Li, C; Lee, TL; Mak, PHS; Fok, SFS; Yang, X; Lau, YL | 2008 | 150 |
| Clinical, Immunological and Molecular Characteristics of 67 Chinese Patients with X-Linked Agammaglobulinemia | Lee, PPW; Chen, TX; Yang, W; Jiang, LP; Chan, KW; Fok, SFS; Lee, TL; Lau, YL | 2008 | 157 |
| The association of RANTES polymorphism with severe acute respiratory syndrome in Hong Kong and Beijing Chinese | Ng, 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, YL | 2007 | 153 |
| Resource of primary immunodeficiency diseases: genetic diagnosis in Hong Kong | Chan, 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, YL | 2007 | 124 |
| Identification of Bruton tyrosine kinase mutations in 12 Chinese patients with X-linked agammaglobulinaemia by long PCR-direct sequencing | Chan, KW; Chen, T; Jiang, L; Fok, SFS; Lee, TL; Lee, BW; Yang, X; Lau, YL | 2006 | 139 |
| Clinical Characteristics and gp91phox Gene Mutations in Seventeen Chinese Children with X-linked Chronic Granulomatous Disease | Lee, PPW; Chan, KW; Lee, TL; Jiang, L; Mak, HS; Fok, SFS; Hui, YF; Li, C; Yang, X; Lau, YL | 2006 | 108 |
| Modulating effects of mannose binding lectin genotype on arterial stiffness in children after Kawasaki disease | Cheung, YF; Ho, MHK; Ip, WK; Fok, SFS; Yung, TC; Lau, YL | 2004 | 103 |
| A Novel Btk Gene Mutation in a Chinese Boy with XLA and Its Carriers | Jiang, LP; Fok, SFS; Wang, LJ; Chan, KW; Wang, M; Liu, EM; Li, X; Deng, B; Yang, XQ; Lau, YL; Toshio, M | 2004 | 95 |
| Mannose-binding lectin and Kawasaki disease in Southern Chinese children | Ho, MHK; Ip, EWK; Cheung, YF; Yung, TC; Cheng, VYW; Fok, SFS; Wong, WHS; Lau, YL | 2003 | 90 |
|
