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2. Notes

3. Index

11. Acknowledgments

13. Contents

16. Cover

17. Notes

18. Frontmatter

19. Index

32. COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report

35. Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development

38. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

39. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

40. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

41. The common variable immunodeficiency IgM repertoire narrowly recognizes erythrocyte and platelet glycans

42. Urine biomarker score captures response to induction therapy with lupus nephritis

44. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

45. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

47. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

49. De novo variants in DENND5B cause a neurodevelopmental disorder

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