Showing results 1 to 2 of 2
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 | 133 | ||
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 | 186 |