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A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13
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The human homologue of yeast CRM1 is in a dynamic subcomplex with CAN/ Nup214 and a novel nuclear pore component Nup88
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Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17p
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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa
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High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones
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The translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNA
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The (6; 9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34
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Can, a putative oncogene associated with myeloid leukemogenesis, can be activated by fusion of its 3′ half to different genes: Characterization of the set gene
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