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Up a levelNumber of items: 5.
Traeger-Synodinos, Joanne, Harteveld, Cornelis L., Old, John M, Petrou, Mary, Galanello, Renzo, Giordano, Piero, Angastioniotis, Michael, De la Salle, Barbara, Henderson, Shirley and May, Alison
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
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Campagna, Dean R., de Bie, Charlotte I., Schmitz-Abe, Klaus, Sweeney, Marion Carol  ORCID: https://orcid.org/0000-0003-0713-0855, Sendamarai, Anoop K., Schmidt, Paul J., Heeney, Matthew M., Yntema, Helger G., Kannengiesser, Caroline, Grandchamp, Bernard, Niemeyer, Charlotte M., Knoers, Nine V. A. M., Swart, Sonia, Marron, Gordon, van Wijk, Richard, Raymakers, Reinier A., May, Alison, Markianos, Kyriacos, Bottomley, Sylvia S., Swinkels, Dorine W. and Fleming, Mark D.
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
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| McCune, Catherine Anne, Al-Jader, Layla N., May, Alison, Hayes, Sara Lindsay, Jackson, Helen A. and Worwood, Mark 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 |
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| Devalia, Vinod, Carter, Kymberley, Walker, Ann P., Perkins, Stephen J., Worwood, Mark, May, Alison and Dooley, James 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 |
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| Culligan, Dominic J., Bowen, David T., May, Alison, White, Denise, Padua, Rose Ann and Burnett, Alan Kenneth 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 |
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