Found: 9
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An unusual fusion gene EML4‐ALK in a patient with congenital mesoblastic nephroma.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 837, doi. 10.1002/gcc.22990
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- Publication type:
- Article
Erratum.
- Published in:
- 2021
- Publication type:
- Correction Notice
Assessing acute myeloid leukemia susceptibility in rearrangement‐driven patients by DNA breakage at topoisomerase II and CCCTC‐binding factor/cohesin binding sites.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 808, doi. 10.1002/gcc.22993
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- Publication type:
- Article
The novel KIT exon 11 germline mutation K558N is associated with gastrointestinal stromal tumor, mastocytosis, and seminoma development.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 827, doi. 10.1002/gcc.22988
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- Publication type:
- Article
Gastrointestinal stromal tumors with BRAF gene fusions. A report of two cases showing low or absent KIT expression resulting in diagnostic pitfalls.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 789, doi. 10.1002/gcc.22991
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- Publication type:
- Article
Aneurysmal bone cyst with an unusual clinical presentation and a novel VDR‐USP6 fusion.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 833, doi. 10.1002/gcc.22989
- By:
- Publication type:
- Article
Recurrent loss of chromosome 22 and SMARCB1 deletion in extra‐axial chordoma: A clinicopathological and molecular analysis.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 796, doi. 10.1002/gcc.22992
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- Publication type:
- Article
Uterine inflammatory myofibroblastic tumor: First report of a ROS1 fusion.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 822, doi. 10.1002/gcc.22986
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- Publication type:
- Article
Issue Information.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 785, doi. 10.1002/gcc.22873
- Publication type:
- Article