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Johnson, B, Lowe, G C, Futterer, J, Lordkipanidze', M, MacDonald, D, Simpson, M A, Sanchez Guiu', I, Drake, S, Bem, D, Leo, V, Fletcher, S J, Dawood, B, Rivera, J, Allsup, D, Biss, T, Bolton-Maggs, P H B, Collins, P, Curry, N, Grimley, C, James, B, Makris, M, Motwani, J, Pavord, S, Talks, K, Thachil, J, Wilde, J, Williams, M, Harrison, P, Gissen, P, Mundell, S J, Mumford, A, Daly, M E, Watson, S P, Morgan, N V 2016, ' Whole Exome Sequencing Identifies Genetic Variants In Inherited Thrombocytopenia With Secondary Qualitative Function Defects ', Haematologica, vol. 101, no. 10, pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316 Johnson, B, Lowe, G C, Futterer, J, Lordkipanidzé, M, Macdonald, D, Simpson, M A, Sanchez-Guiú, I, Drake, S, Bem, D, Leo, V, Fletcher, S J, Dawood, B, Rivera, J, Allsup, D, Biss, T, Bolton-Maggs, P H, Collins, P, Curry, N, Grimley, C, James, B, Makris, M, Motwani, J, Pavord, S, Talks, K, Thachil, J, Wilde, J, Williams, M, Harrison, P, Gissen, P, Mundell, S, Mumford, A, Daly, M E, Watson, S P & Morgan, N V 2016, ' Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects ', Haematologica, vol. 101, no. 10, pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316