| P2093 | author name string | M Perić | |
| | H Šahović | |
| | S Mešanović | |
| P2860 | cites work | Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: a study of 106 cases. | Q50945096 |
| | Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system. | Q51023659 |
| | Prognostic factors in idiopathic (primary) osteomyelofibrosis | Q73605917 |
| | Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia | Q78365656 |
| | The translocation (4;12)(q31;q21) in myelofibrosis associated with myelodysplastic syndrome: impact of the 12q21 breakpoint | Q81644830 |
| | Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis | Q29614337 |
| | A gain-of-function mutation of JAK2 in myeloproliferative disorders | Q29618851 |
| | Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders | Q29618853 |
| | Chronic idiopathic myelofibrosis: clinicopathologic features, pathogenesis, and prognosis | Q33252344 |
| | The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes | Q35848032 |
| | Idiopathic myelofibrosis in blast transformation with 4;12 and 5;12 translocations and a 7q deletion | Q45048857 |
| | Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders | Q46513376 |
| | EVI1 is consistently expressed as principal transcript in common and rare recurrent 3q26 rearrangements | Q49097152 |
| P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported | Q19125045 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P921 | main subject | chronic idiopathic myelofibrosis | Q3857106 |
| P304 | page(s) | 63-68 | |
| P577 | publication date | 2014-06-01 | |
| P1433 | published in | Balkan Journal of Medical Genetics | Q15750519 |
| P1476 | title | Translocation t(3;12)(q26;q21) in JAK2(V617F) Point Mutation Negative Chronic Idiopathic Myelofibrosis: A Case Report | |
| P478 | volume | 17 | |