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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1980 | 1 |
1998 | 1 |
2005 | 2 |
2023 | 0 |
PubMed (OMIM) for id: 10146
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A gain-of-function mutation of JAK2 in myeloproliferative disorders.
N Engl J Med. 2005 Apr 28;352(17):1779-90. doi: 10.1056/NEJMoa051113.
N Engl J Med. 2005.
PMID: 15858187
Free article.
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.
Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, Vassiliou GS, Bench AJ, Boyd EM, Curtin N, Scott MA, Erber WN, Green AR; Cancer Genome Project.
Baxter EJ, et al.
Lancet. 2005 Mar 19-25;365(9464):1054-61. doi: 10.1016/S0140-6736(05)71142-9.
Lancet. 2005.
PMID: 15781101
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Familial idiopathic myelofibrosis and multiple hemangiomas.
Bonduel M, Sciuccati G, Torres AF, Pierini A, Gallo G.
Bonduel M, et al.
Am J Hematol. 1998 Oct;59(2):175-7. doi: 10.1002/(sici)1096-8652(199810)59:2<175::aid-ajh13>3.0.co;2-8.
Am J Hematol. 1998.
PMID: 9766805
Free article.
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Familial myelofibrosis.
Sieff CA, Malleson P.
Sieff CA, et al.
Arch Dis Child. 1980 Nov;55(11):888-93. doi: 10.1136/adc.55.11.888.
Arch Dis Child. 1980.
PMID: 7436463
Free PMC article.
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