Pseudo-Pelger–Huët anomaly and granulocytic dysplasia associated with human granulocytic anaplasmosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-015-1769-1.pdf
Reference26 articles.
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3. Hoffmann K, Dreger CK, Olins AL, et al. Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huet anomaly). Nat Genet. 2002;31:410–4.
4. Best S, Salvati F, Kallo J, et al. Lamin B-receptor mutations in Pelger–Huët anomaly. Br J Haematol. 2003;123:542–4.
5. Economopoulou C, Pappa V, Kontsioti F, et al. Analysis of apoptosis regulatory gene expression in the bone marrow (BM) of adult de novo myelodysplastic syndromes (MDS). Leuk Res. 2008;32:61–9.
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