Showing results 3 to 7 of 7
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Title | Author(s) | Issue Date | Views | |
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Molecular Analysis of 12 Chinese patients with X-linked Hyper-IgM syndrome Proceeding/Conference:Keystone Symposia on Human Immunology and Immunodeficiencies | 2009 | 133 | ||
Identify a Novel CYBB Gene Mutation in a Chinese Boy with X-Linked Chronic Granulomer Disease and Its Carriers Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | 130 | ||
Identify a Novel Btk Splice Site Mutation in a Chinese Boy with XLA Proceeding/Conference:Hong Kong Journal of Paediatrics | 2004 | 127 | ||
Genotype-Phenotype Correlation Study in 62 Patients with X-Linked Agammaglobulinemia Human Immunology and Immunodeficiencies Proceeding/Conference:Keystone Symposium on Human Immunology and Immunodeficiencies | 2009 | 128 | ||
Clinical and Molecular Characteristics of 32 Chinese Children with Wiskott-Aldrich Syndrome Proceeding/Conference:Keystone symposium on Human Immunology and Immunodeficiencies | 2009 | 110 |