Melanie J. Percy
Department of Haematology
Belfast City Hospital
Belfast
United Kingdom
Name/email consistency: high
- Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Percy, M.J., Rumi, E. Am. J. Hematol. (2009)
- A gain-of-function mutation in the HIF2A gene in familial erythrocytosis. Percy, M.J., Furlow, P.W., Lucas, G.S., Li, X., Lappin, T.R., McMullin, M.F., Lee, F.S. N. Engl. J. Med. (2008)
- Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis. Percy, M.J., Beer, P.A., Campbell, G., Dekker, A.W., Green, A.R., Oscier, D., Rainey, M.G., van Wijk, R., Wood, M., Lappin, T.R., McMullin, M.F., Lee, F.S. Blood (2008)
- Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency. Percy, M.J., Lappin, T.R. Br. J. Haematol. (2008)
- A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove. Percy, M.J., Furlow, P.W., Beer, P.A., Lappin, T.R., McMullin, M.F., Lee, F.S. Blood (2007)
