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Article

HLA-matched related-donor HSCT in Fanconi anemia patients conditioned with cyclophosphamide and fludarabine

8 Jan 2015

Abstract excerpt

To the editor: Fanconi anemia (FA) is a rare, phenotypically heterogeneous inherited disorder clinically characterized by congenital abnormalities, progressive bone marrow failure (BMF), and a predisposition to develop malignancies.[1][1] Hematopoietic stem cell transplantation (HSCT) is the only

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Identifiers

PMID: 25573976
DOI: 10.1182/blood-2014-10-605113

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