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1. European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia

2. Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia

3. A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery

4. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

6. Impact of newborn screening for SCID on the management of congenital athymia

8. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

10. Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study

11. Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK

14. Erythropoiesis defect observed in STAT3 GOF patients with severe anemia

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