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TypeTitleAuthor(s)YearViews
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
 
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, YL2010226
 
A new autosomal recessive, heterozygous pair of mutations of CYBA in a patient with chronic granulomatous diseaseChang, YH; Yu, HH; Lau, YL; Chan, KW; Chiang, BL201064
 
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, YL2009184
 
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