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August 15, 1998Blood

The t(8;13) Atypical Myeloproliferative Disorder: Further Analysis of the ZNF198 Gene and Lack of Evidence for Multiple Genes Disrupted on Chromosome 13

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Authors

ISIvan H. StillRoswell Park Comprehensive Cancer CenterJCJohn K. CowellNational Cancer Center of Georgia

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Still et al. (1998) studied this question.

synapsesocial.com/papers/6a204ed4e9ca693ff1e71f70https://doi.org/10.1182/blood.v92.4.1456.spll3_1456_1458
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder1998 · 15 citations
  2. 2Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization1998 · 13 citations
  3. 3Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome 131995 · 26 citations
  4. 4A syndrome of lymphoblastic lymphoma, eosinophilia, and myeloid hyperplasia/malignancy associated with t(8;13)(p11;q11): description of a distinctive clinicopathologic entity [see comments]1995 · 142 citations
  5. 5Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12)1998 · 156 citations