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Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis
UploadT-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication
Download from doi.orgUpdate on the use of immunoglobulin in human disease: A review of evidence
UploadPrimary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
Download from europepmc.orgBiallelic mutations in IRF8 impair human NK cell maturation and function
Download from doi.orgDestabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease
Download from doi.orgCopa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease
Download from link.springer.comMutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder
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