Associated Papers
Novel mutations in hyper-IgM syndrome type 2 and X-linked agammaglobulinemia detected in three patients with primary immunodeficiency disease.
Chen X et al.
Molecular Genetics & Genomic Medicine, 2021
Spatial intratumoral heterogeneity and temporal clonal evolution in esophageal squamous cell carcinoma.
Hao JJ et al.
Nature Genetics, 2016
27749841 (PubMed )
Supplement: NIHMS814330-supplement-4.xlsx › Sheet1
Hyper IgM Syndrome Type 2 Presenting as Intestinal Lymphoid Polyposis Without Recurrent Infection.
de la Varga-Martínez R et al.
Journal of Investigational Allergology & Clinical Immunology, 0
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