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15. Contributors

16. List of contributors

17. Experiences and Attitudes Toward Telemedicine in an Adult Congenital Heart Disease Clinic: Lessons Learned from the COVID-19 Pandemic

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

19. 108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns

25. De novo variants in DENND5B cause a neurodevelopmental disorder

27. Humoral And Cellular Immune Response To Covid-19 Vaccines After Primary Vaccination With A 3-dose Scheme And Boosters Vaccines (4th And 5th Doses) In 55 Brazilian Patients With Inborn Errors Of Immunity Compared To Healthy Controls

29. Contributors

31. Long-term sustainability of ecological monitoring

34. Contributors

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

37. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

44. Emapalumab for the treatment of refractory cytokine release syndrome in pediatric patients

47. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

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