Referral centre variation in requestingJAK2V617F mutation analysis for the investigation of a myeloproliferative neoplasm
Author:
Publisher
BMJ
Subject
General Medicine,Pathology and Forensic Medicine
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A molecular diagnostic algorithm for JAK2 V617F investigations in suspected myeloproliferative neoplasms;Irish Journal of Medical Science (1971 -);2019-10-25
2. An increase in diagnostic JAK2 V617F mutation testing: Is masked polycythaemia vera the explanantion?;European Journal of Internal Medicine;2018-06
3. Neutrophilia and the JAK2 V617F Mutation;Pathology & Oncology Research;2017-09-24
4. Who to screen for calreticulin mutations? An audit of real-life practice and review of current evidence;European Journal of Internal Medicine;2017-05
5. In Response to “BCR-ABL Testing by Polymerase Chain Reaction in Patients With Neutrophilia: The William Beaumont Hospital Experience and the Case for Rational Laboratory Test Requests”;Journal of Oncology Practice;2017-04
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