Cyhoeddiadau
2015
- Traeger-Synodinos, J. et al. 2015. EMQN best practice guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies. European Journal of Human Genetics 23(4), pp. 426-437. (10.1038/ejhg.2014.131)
2014
- Campagna, D. R. et al. 2014. X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations. American Journal of Hematology 89(3), pp. 315-319. (10.1002/ajh.23616)
2002
- McCune, C. A., Al-Jader, L. N., May, A., Hayes, S. L., Jackson, H. A. and Worwood, M. 2002. Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload. Human Genetics 111(6), pp. 538-543. (10.1007/s00439-002-0824-1)
- Devalia, V., Carter, K., Walker, A. P., Perkins, S. J., Worwood, M., May, A. and Dooley, J. S. 2002. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). Blood 100(2), pp. 695-697. (10.1182/blood-2001-11-0132)
1995
- Culligan, D. J., Bowen, D. T., May, A., White, D., Padua, R. A. and Burnett, A. K. 1995. Refractory anaemia with preleukaemic polyclonal haemopoiesis and the emergence of monoclonal erythropoiesis on disease progression. British Journal of Haematology 89(3), pp. 675-677. (10.1111/j.1365-2141.1995.tb08389.x)