Showing 1 - 4 results of 4 for search 'Annabel Maclachlan', query time: 0.02s
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Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function by Annabel Maclachlan, Gerry Dolan, Charlotte Grimley, Steve P. Watson, Neil V. Morgan, on behalf of the UK GAPP Study Group
Published 2017-08-01
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Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis by Rashid Al Ghaithi, Jun Mori, Zoltan Nagy, Annabel Maclachlan, Lewis Hardy, Helen Philippou, Emma Hethershaw, Neil V. Morgan, Yotis A. Senis, Paul Harrison
Published 2019-10-01
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Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding by Gillian C. Lowe, Roksana Fickowska, Rashid Al Ghaithi, Annabel Maclachlan, Paul Harrison, Will Lester, Steve P. Watson, Bethan Myers, Justin Clark, Neil V. Morgan
Published 2019-01-01
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