Items where authors include "Goodeve, A.C."
Article
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. orcid.org/0000-0002-6177-7062 (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. orcid.org/0000-0002-1387-8926, 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