The c.64 + 2 T > A Founder Variant Hits Home: Report on 14 Patients Expands the Phenotypic Landscape of Inherited ARPC1B Deficiency – a Comparative Analysis
Acute Non-Promyelocytic Leukemia with Complex Karyotype and Novel t (15;17) (q21; p11.2)/B2M: RARA Fusion: A Case Report
