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2. Bone Density and Fractures in Autosomal Dominant Hyper IgE Syndrome

3. Lung Parenchyma Surgery in Autosomal Dominant Hyper-IgE Syndrome

6. Coronary Artery Abnormalities in Hyper-IgE Syndrome

7. Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

8. Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome

9. Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

10. Mutant deoxynucleotide carrier is associated with congenital microcephaly

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