Whole exome sequencing in patients with inherited thrombocytopenia and excessive bleeding is an efficient way to identify genetic variants in known and novel genes

Johnson, B; Lowe, G; Simpson, M; Guiu, IS; Drake, S; MacDonald, D; Bem, D; Fletcher, S; Futterer, J; Leo, V; Lordkipanidze, M; Dawood, B; Biss, T; Bolton-Maggs, P; Collins, P; Curry, N; Makris, M; Motwani, J; Pavord, S; Talks, K; Thacil, J; Wilde, J; Williams, M; Harrison, P; Gissen, P; Mundell, S; Mumford, A; Daly, M; Watson, S; Morgan, N; UK-GAPP, Study, Grp

doi:10.1111/jth.12993

Whole exome sequencing in patients with inherited thrombocytopenia and excessive bleeding is an efficient way to identify genetic variants in known and novel genes

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Author(s): Johnson B, Lowe G, Simpson M, Guiu IS, Drake S, MacDonald D, Bem D, Fletcher S, Futterer J, Leo V, Lordkipanidze M, Dawood B, Biss T, Bolton-Maggs P, Collins P, Curry N, Makris M, Motwani J, Pavord S, Talks K, Thacil J, Wilde J, Williams M, Harrison P, Gissen P, Mundell S, Mumford A, Daly M, Watson S, Morgan N, UK-GAPP Study Grp

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: XXV Congress of the International Society on Thrombosis and Haemostasis

Year of Conference: 2015

Pages: 19-19

Print publication date: 01/06/2015

Acceptance date: 01/01/1900

Publisher: Wiley-Blackwell Publishing Ltd.

URL: http://dx.doi.org/10.1111/jth.12993

DOI: 10.1111/jth.12993

Series Title: Journal of Thrombosis and Haemostasis

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Whole exome sequencing in patients with inherited thrombocytopenia and excessive bleeding is an efficient way to identify genetic variants in known and novel genes

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