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Human Pathology
Volume 41, Issue 5
, Pages
758-762
, May 2010
JAK2 V617F mutation is uncommon in patients with the 3q21q26 syndrome
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PII: S0046-8177(09)00407-9
doi: 10.1016/j.humpath.2009.11.004
© 2010 Elsevier Inc. All rights reserved.
« Previous
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Human Pathology
Volume 41, Issue 5
, Pages
758-762
, May 2010
