IMMUNOSUPPRESSIVE THERAPY IN A PATIENT WITH SAA-like RCC AND GATA2 DEFICIENCY by D Kroiss, W Novak, S Karlhuber, G Engstler, H Boztug, M Dworzak

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PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY by J. Berner, W. Novak, R. Jimenez-Heredia, L. Kager, K. Boztug

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P1046: SEVERE COMPLICATIONS IN JAK2 V617F POSITIVE PEDIATRIC PATIENTS WITH MYELOPROLIFERATIVE NEOPLASMS by W. Novak, C. Annamária, R. Crazzolara, J. Neil, K. Pirolt, M. Dworzak, L. Kager

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Rare Presentation of Small Bowel Obstruction Secondary to Intestinal Leiomyoma in a Patient with Crohn’s Disease by Benjamin J. Behers, Brett M. Behers, Ryan C. Perez, Kabir Grewal, Joe Cyriac, Joanne Makar, Russell W. Novak

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P1531: HETEROGENEITY OF DISEASE-CAUSING GENOTYPES BETWEEN FAMILIES WITH HEREDITARY SPHEROCYTOSIS: A SINGLE-CENTER COHORT STUDY by R. Jimenez Heredia, L. Kager, P. Zeitlhofer, W. Novak, S. Eder, A. Segarra Roca, K. Nebral, M. Haimel, R. Geyeregger, O. Haas, K. Boztug

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