Showing results 7 to 11 of 11
< previous
Title | Author(s) | Issue Date | |
---|---|---|---|
Molecular Analysis of 12 Chinese patients with X-linked Hyper-IgM syndrome Proceeding/Conference:Keystone Symposia 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 | ||
A Novel Btk Gene Mutation in a Chinese Boy with XLA and Its Carriers Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | ||
Two Novel ITGB2 Gene Mutations in a Chinese Boy with Leucocyte Adhesion Deficiency Type 1 Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | ||
Unique pattern of infections in chronic granulomatous disease – The Asian experience Proceeding/Conference:ASPR / PSM 2013 Joint Scientific Meeting | 2013 |