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. 2012 May;20(5).

doi: 10.1038/ejhg.2011.252. Epub 2012 Jan 25.

Clinical utility gene card for: familial erythrocytosis

Kais Hussein¹, Melanie Percy, Mary Frances McMullin

Affiliations

PMID: 22274579
PMCID: PMC3330227
DOI: 10.1038/ejhg.2011.252

Clinical utility gene card for: familial erythrocytosis

Kais Hussein et al. Eur J Hum Genet. 2012 May.

. 2012 May;20(5).

doi: 10.1038/ejhg.2011.252. Epub 2012 Jan 25.

Authors

Kais Hussein¹, Melanie Percy, Mary Frances McMullin

Affiliation

¹ Institute of Pathology, Hannover Medical School, Hannover, Germany. Hussein.Kais@mh-hannover.de

PMID: 22274579
PMCID: PMC3330227
DOI: 10.1038/ejhg.2011.252

No abstract available

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References

1. McMullin MF. Idiopathic erythrocytosis: a disappearing entity. Hematology Am Soc Hematol Educ Program. 2009;1:629–635. - PubMed
1. Percy MJ, Rumi E. Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol. 2009;84:46–54. - PubMed
1. Gordeuk VR, Stockton DW, Prchal JT. Congenital polycythemias/erythrocytoses. Haematologica. 2005;90:109–116. - PubMed
1. Rives S, Pahl HL, Florensa L, et al. Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis. Haematologica. 2007;92:674–677. - PubMed
1. Ang SO, Chen H, Gordeuk VR, et al. Endemic polycythemia in Russia: mutation in the VHL gene. Blood Cells Mol Dis. 2002;28:57–62. - PubMed

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