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Article

Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes.

British journal of haematology - 1 Jan 2014

Babushok Daria V, Xie Hongbo M, Roth Jacquelyn J, Perdigones Nieves, Olson Timothy S, Cockroft Joshua D, Gai Xiaowu, Perin Juan C, Li Yimei, Paessler Michele E, Hakonarson Hakon, Podsakoff Gregory M, Mason Philip J, Biegel Jaclyn A, Bessler Monica

Abstract excerpt

The bone marrow failure syndromes (BMFS) are a heterogeneous group of rare blood disorders characterized by inadequate haematopoiesis, clonal evolution, and increased risk of leukaemia. Single nucleotide polymorphism arrays (SNP-A) have been proposed as a tool for surveillance of clonal evolution in BMFS. To better understand the natural history of BMFS and to assess the clinical utility of SNP-A in these...

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Identifiers

PMID: 24116929
DOI: 10.1111/bjh.12603
PMCID: PMC3986350

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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