Showing results 1 to 5 of 5
| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Molecular Analysis of 12 Chinese patients with X-linked Hyper-IgM syndrome Proceeding/Conference:Keystone Symposia on Human Immunology and Immunodeficiencies | 2009 | 169 | ||
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 | 203 | ||
| 2011 | 242 | |||
Resource of primary immunodeficiency diseases: genetic diagnosis in Hong Kong Proceeding/Conference:International Congress of Pediatrics, IPA 2007 | 2007 | 136 | ||
Unique pattern of infections in chronic granulomatous disease – The Asian experience Proceeding/Conference:ASPR / PSM 2013 Joint Scientific Meeting | 2013 | 109 |