Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12)

Chromosome 8p11–12 is the site of a recurrent breakpoint in a myeloproliferative disorder that involves lymphoid (T- or B-cell), myeloid hyperplasia and eosinophilia, and evolves toward acute leukemia. This multilineage involvement suggests the malignant transformation of a primitive hematopoietic s...

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Main Authors: Popovici, Cornel, Adélaïde, José, Ollendorff, Vincent, Chaffanet, Max, Guasch, Géraldine, Jacrot, Michèle, Leroux, Dominique, Birnbaum, Daniel, Pébusque, Marie-Josèphe
Formáid: Artigo
Teanga:Inglês
Foilsithe: National Academy of Sciences 1998
Ábhair:
Biological Sciences
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC20444/
https://ncbi.nlm.nih.gov/pubmed/9576949
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