Showing results 1 to 6 of 6
Title | Author(s) | Issue Date | |
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Clinical and molecular characteristics of 35 chinese children with wiskott-aldrich syndrome Journal:Journal of Clinical Immunology | 2009 | ||
Inherited Defects in Interleukin-12/Interferon-gamma Pathway in Patients with Unusual Mycobacterial Infections Proceeding/Conference:Keystone Symposium on Human Immunology and Immunodeficiencies | 2009 | ||
Molecular diagnosis of severe combined immunodeficiency - Identification of IL2RG, JAK3, IL7R, DCLRE1C and RAG2 mutations in a cohort of Chinese and Southeast Asian children Proceeding/Conference:Congress of Asian Society for Pediatric Research & AM of Taiwan Pediatric Association | 2010 | ||
2011 | |||
Severe mycobacterial infections in two pairs of Chinese siblings with interleukin-12 receptor β1 deficiency Journal:European Journal of Pediatrics | 2008 | ||
嚴重聯合免疫缺陷病 I 例基因診斷及家系分析 Proceeding/Conference:江、浙、滬兒科學術會會議 | 2007 |