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8p11 Myeloproliferative syndrome with t(8;22)(p11;q11): A case report
The 8p11 myeloproliferative syndrome (EMS), a rare myeloproliferative disease, generally progresses rapidly and is characterized by chromosomal translocations of the fibroblast growth factor receptor 1 (FGFR1) gene. The FGFR1 gene is located at chromosome 8p11 and may fuse with distinct partner gene...
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| Foilsithe in: | Exp Ther Med |
|---|---|
| Main Authors: | , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
D.A. Spandidos
2018
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6090294/ https://ncbi.nlm.nih.gov/pubmed/30116393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2018.6328 |
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