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Number of items: 7.

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

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