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Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis.
Gene interactions and stroke risk in children with sickle cell anemia.
Deferiprone and hepatic fibrosis.
Prenatal origin of childhood acute myeloid leukemias harboring chromosomal rearrangements t(15;17) and inv(16).
Distinct HLA associations by stroke subtype in children with sickle cell anemia.
Hematologic effects of inactivating the Ras processing enzyme Rce1.
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease.
Comprehensive banking of sibling donor cord blood for children with malignant and nonmalignant disease.
Retroviral transduction of IL2RG into CD34(+) cells from X-linked severe combined immunodeficiency patients permits human T- and B-cell development in sheep chimeras.
Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease.