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Article

The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1

31 Mar 2005

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Share to Chronic Myeloid Leukemia Treatments
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15800673
DOI: 10.1038/sj.leu.2403712

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Related research

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The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1PMID 15800673Read ↗

Identification of a <i>MYO18A‐PDGFRB</i> fusion gene in an eosinophilia‐associated atypical myeloproliferative neoplasm with a t(5;17)(q33‐34;q11.2)Semantic proximity Read ↗

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The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25Semantic proximity Read ↗

8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes.Semantic proximity Read ↗

A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: Case report and review of literatureSemantic proximity Read ↗

Clinical and genomic profiling of a patient with a de novo ring chromosome 18: A case report highlighting autoimmune and neurological implicationsSemantic proximity Read ↗

LRRFIP1, a new FGFR1 partner gene associated with 8p11 myeloproliferative syndromeSemantic proximity Read ↗

Identification of a novel partner gene, <i>TPR</i>, fused to <i>FGFR1</i> in 8p11 myeloproliferative syndromeSemantic proximity Read ↗

KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.Semantic proximity Read ↗

Fibroblast growth factor receptor-4 splice variants cause deletion of a critical tyrosine.Semantic proximity Read ↗

Identification of four new translocations involving FGFR1 in myeloid disordersSemantic proximity Read ↗

C to A single nucleotide polymorphism in intron 18 of the human MST1R (RON) gene that maps at 3p21.3.Semantic proximity Read ↗

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