Testing for hereditary spherocytosis: a French experience
- PMID: 23204481
- PMCID: PMC3590076
- DOI: 10.3324/haematol.2012.074070
Testing for hereditary spherocytosis: a French experience
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Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.Haematologica. 2012 Apr;97(4):516-23. doi: 10.3324/haematol.2011.052845. Epub 2011 Nov 4. Haematologica. 2012. PMID: 22058213 Free PMC article.
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- Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ. General Haematology Task Force of the British Committee for Standards in Haematology. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update. Br J Haematol. 2012;156(1):37-49 - PubMed
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- Girodon F, Garçon L, Bergoin E, Largier M, Delaunay J, Fénéant-Thibault M, et al. Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis. Br J Haematol. 2008;140(4):468-70 - PubMed
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