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Number of items: 7.


Cartwright, A., Peake, I.R., Goodeve, A.C. et al. (1 more author) (2016) In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion. Haemophilia. ISSN 1351-8216

Edison, E., Konkle, B.A. and Goodeve, A.C. (2016) Genetic analysis of bleeding disorders. Haemophilia, 22 (S5). pp. 79-83. ISSN 1351-8216

Simeoni, I., Stephens, J.C., Hu, F. et al. (76 more authors) (2016) A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders. Blood, 127 (23). pp. 2791-2803. ISSN 0006-4971

Flood, V.H., Christopherson, P.A., Gill, J.C. et al. (22 more authors) (2016) Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States. Blood, 127 (20). pp. 2481-2488. ISSN 0006-4971

Stockley, J., Nisar, S.P., Leo, V.C. et al. (9 more authors) (2015) Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease. PLoS ONE, 10 (12). e0143913. ISSN 1932-6203

Goodeve, A.C. (2015) Hemophilia B: Molecular pathogenesis and mutation analysis. Journal of Thrombosis and Haemostasis, 13 (7). pp. 1184-1195. ISSN 1538-7933

Hampshire, D.J., Abuzenadah, A.M., Cartwright, A. et al. (10 more authors) (2013) Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort. Thrombosis and Haemostasis, 110 (2). pp. 264-274. ISSN 0340-6245

This list was generated on Sun Oct 20 19:41:00 2019 BST.