PedAM
Pediatric Disease Annotations & Medicines
| Disease | myeloid leukemia |
| Phenotype | C0001815|primary myelofibrosis |
| Sentences | 1 |
| PubMedID- 24315414 | We report the molecular cloning and functional characterization of a novel fgfr1op (exon 11)-ret (exon 11) gene fusion event (named fgfr1op-ret), mediated by a reciprocal translocation t(6; 10)(q27; q11), in a patient affected by primary myelofibrosis (pmf) with secondary acute myeloid leukemia (aml). |
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