Items where authors include "Lowe, G.C."

Article

Johnson, B., Doak, R., Allsup, D. et al. (15 more authors) (2018) A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia. Research and Practice in Thrombosis and Haemostasis, 2 (4). pp. 640-652. ISSN 2475-0379

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Jones, M.L., Norman, J.E., Morgan, N.V. et al. (9 more authors) (2016) Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors. THROMBOSIS AND HAEMOSTASIS, 113 (4). pp. 826-837. ISSN 0340-6245

Fletcher, S.J., Johnson, B., Lowe, G.C. et al. (12 more authors) (2015) SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. Journal of Clinical Investigation, 125 (9). 3600 - 3605. ISSN 0021-9738

Leo, V.C., Morgan, N.V., Bem, D. et al. (9 more authors) (2015) Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. Journal of Thrombosis and Haemostasis, 13 (4). pp. 643-650. ISSN 1538-7933