Items where authors include "Hampshire, D.J."

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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

Ali, S., Shetty, S., Ghosh, K. et al. (5 more authors) (2016) Congenital macrothrombocytopenia is a heterogeneous disorder in India. Haemophilia, 22 (4). pp. 570-582. 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

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

Leal, G.F., Roberts, E., Silva, E.O. et al. (3 more authors) (2003) A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2. Journal of Medical Genetics, 40 (7). pp. 540-542. ISSN 0022-2593

Roberts, E., Hampshire, D.J., Pattison, L. et al. (8 more authors) (2002) Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. Journal of Medical Genetics, 39 (10). pp. 718-721. ISSN 0022-2593

Hampshire, D.J., Roberts, E., Crow, Y. et al. (5 more authors) (2001) Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. Journal of Medical Genetics, 38 (10). pp. 680-682. ISSN 0022-2593

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