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Article

JAK2 V617F mutation is uncommon in patients with the 3q21q26 syndrome.

Human pathology - 1 May 2010

Lin Pei, Luthra Rajyalakshmi, Nussenzveig Roberto H, Medeiros L Jeffrey

Abstract excerpt

The 3q21q26 syndrome is recognized as a distinct clinicopathologic entity. Patients have a myeloid neoplasm associated with 3q21q26 cytogenetic abnormalities and present with anemia, leukopenia, and either thrombocytosis or a normal platelet count associated with dysplasia. To determine if JAK2 V617F mutation is implicated in the abnormal thrombopoiesis of the 3q21q26 syndrome, we analyzed bone marrow samples of...

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Source

Identifiers

PMID: 20153505
DOI: 10.1016/j.humpath.2009.11.004

Genes

JAK2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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