Young people with Sickle Cell Disorder and education: A knowledge review

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dc.contributor.authorAbuateya, Hala
dc.contributor.authorAtkin, Karl
dc.contributor.authorCulley, Lorraine
dc.contributor.authorDyson, Sue, 1960-
dc.contributor.authorDyson, Simon
dc.date.accessioned2009-10-01T09:47:55Z
dc.date.available2009-10-01T09:47:55Z
dc.date.issued2008
dc.identifier.citationAbuateya, H, Atkin, K, Culey L, Dyson Sue, Dyson, S Young People with Sickle Cell Disorder and Education: A Knowledge Review . Diversity in Health and Social Care, 5 (2)en
dc.identifier.issn1759-1422
dc.identifier.issn1759-1430
dc.identifier.urihttp://hdl.handle.net/2086/2697
dc.language.isoenen
dc.researchgroupUnit for the Social Study of Thalassaemia and Sickle Cell
dc.researchgroupReproduction Research Group
dc.researchgroupMary Seacole Research Centre
dc.researchgroupNursing and Midwifery Research Centre
dc.researchgroupHealth Policy Research Unit
dc.researchinstituteInstitute for Allied Health Sciences Researchen
dc.researchinstituteCentre for Reproduction Research (CRR)en
dc.titleYoung people with Sickle Cell Disorder and education: A knowledge reviewen
dc.typeArticleen

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