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JAK2 V617F mutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes.

Blood Adv · 2023 · PMC10758737 · PMID 38011490

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Similar trends were noted for all MF subtypes, which did not reach statistical significance in all cases, possibly owing to the small sample size.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.