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Editorial
. 2000 May 20;320(7246):1353-4.
doi: 10.1136/bmj.320.7246.1353.

A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports

A Streetly
Editorial

A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports

A Streetly. BMJ. .
No abstract available

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References

    1. Streetly A, Maxwell K, Mejia A. Sickle cell disorder in Greater London: a needs assessment of screening and care services. Fair shares for London. London: United Medical and Dental Schools, Department of Public Health Medicine; 1997.
    1. Modell B, Petrou M, Layton M, Varvanides L, Slater C, Ward RHT, et al. Status report: audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years. BMJ. 1997;315:779–782. - PMC - PubMed
    1. Modell B, Harris R, Lowe B, Khan M, Darlinson M, Petrou M, et al. Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential enquiry. BMJ. 2000;320:337–341. - PMC - PubMed
    1. NHS Executive. London: Department of Health; 1999. Standing Medical Advisory Committee Working Party Report on sickle cell, thalassaemia and other haemoglobinopathies.
    1. Davies SC, Cronin E, Gill M, Greengross P, Hickman M, Normand C. Screening for sickle cell disease and thalassaemia—a systematic review with supplementary research. Health Technol Assess 2000;4(3). - PubMed

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