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Mutational profiling in suspected triple-negative essential thrombocythaemia using targeted next-generation sequencing in a real-world cohort.
Michail O, McCallion P, McGimpsey J, Hindley A, Greenfield G, McAllister R, Feerick J, Arnold C, Cross N, Cuthbert R, McMullin MF, Catherwood MA. Michail O, et al. Among authors: mcmullin mf. J Clin Pathol. 2021 Dec;74(12):808-811. doi: 10.1136/jclinpath-2020-206570. Epub 2020 Nov 3. J Clin Pathol. 2021. PMID: 33144355
Hereditary thrombocytosis: the genetic landscape.
Han EY, Catherwood M, McMullin MF. Han EY, et al. Among authors: mcmullin mf. Br J Haematol. 2021 Sep;194(6):1098-1105. doi: 10.1111/bjh.17741. Epub 2021 Aug 2. Br J Haematol. 2021. PMID: 34341988 No abstract available.
Significance of NPM1 Gene Mutations in AML.
Hindley A, Catherwood MA, McMullin MF, Mills KI. Hindley A, et al. Among authors: mcmullin mf. Int J Mol Sci. 2021 Sep 17;22(18):10040. doi: 10.3390/ijms221810040. Int J Mol Sci. 2021. PMID: 34576201 Free PMC article. Review.
269 results