Works matching IS 10452257 AND DT 2020 AND VI 59 AND IP 7
Results: 7
A novel MBTD1‐PHF1 gene fusion in endometrial stromal sarcoma: A case report and literature review.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 428, doi. 10.1002/gcc.22845
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- Publication type:
- Article
Table of Content Volume 59, Number 7, July 2020.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 387, doi. 10.1002/gcc.22775
- Publication type:
- Article
Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 396, doi. 10.1002/gcc.22841
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- Article
Identification of a t(X;17)(q28;q21) generating a KANSL1‐MTCP1 gene fusion leading to dysregulated expression of MTCP1 in acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 417, doi. 10.1002/gcc.22840
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- Article
Variant WWTR1 gene fusions in epithelioid hemangioendothelioma—A genetic subset associated with cardiac involvement.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 389, doi. 10.1002/gcc.22839
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- Publication type:
- Article
Immuno‐oncology gene expression profiling of formalin‐fixed and paraffin‐embedded clear cell renal cell carcinoma: Performance comparison of the NanoString nCounter technology with targeted RNA sequencing.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 406, doi. 10.1002/gcc.22843
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- Article
Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 422, doi. 10.1002/gcc.22842
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- Publication type:
- Article