Works matching IS 10452257 AND DT 2022 AND VI 61 AND IP 1
Results: 9
Transcriptome sequencing of archived lymphoma specimens is feasible and clinically relevant using exome capture technology.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 27, doi. 10.1002/gcc.23002
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- Article
Ovarian germ cell tumor/mastocytosis with KIT mutation: A unique clinicopathological entity.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 50, doi. 10.1002/gcc.23000
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- Article
Undifferentiated sarcoma of bone with a round to epithelioid cell phenotype harboring a novel EWSR1‐SSX2 fusion identified by RNA‐based next‐generation sequencing.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 44, doi. 10.1002/gcc.22999
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- Article
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 22, doi. 10.1002/gcc.22998
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- Article
Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma: A potential treatment target in rare cases?
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 5, doi. 10.1002/gcc.22996
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- Article
Sustained remission after ruxolitinib and chimeric antigen receptor T‐cell therapy bridged to a second allogeneic hematopoietic stem cell transplantation for relapsed Philadelphia chromosome‐like B‐cell precursor acute lymphoblastic leukemia with novel NPHP3‐JAK2 fusion
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 55, doi. 10.1002/gcc.22995
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- Article
Issue Information.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 1, doi. 10.1002/gcc.22958
- Publication type:
- Article
Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 10, doi. 10.1002/gcc.22997
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- Article
Balanced and unbalanced translocations in a multicentric series of 2843 patients with chronic lymphocytic leukemia.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 1, p. 37, doi. 10.1002/gcc.22994
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- Article