Works matching IS 10452257 AND DT 2020 AND VI 59 AND IP 2
Results: 8
Multifocal primary neuroblastoma tumor heterogeneity in siblings with co‐occurring PHOX2B and NF1 genetic aberrations.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 119, doi. 10.1002/gcc.22809
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- Article
Cryptic recurrent ACIN1‐NUTM1 fusions in non‐KMT2A‐rearranged infant acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 125, doi. 10.1002/gcc.22808
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- Article
Detection of CSF1 rearrangements deleting the 3′ UTR in tenosynovial giant cell tumors.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 96, doi. 10.1002/gcc.22807
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- Article
Identification of new hypoxia‐regulated epithelial‐mesenchymal transition marker genes labeled by H3K4 acetylation.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 73, doi. 10.1002/gcc.22802
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- Article
Insertional oncogenesis by HPV70 revealed by multiple genomic analyses in a clinically HPV‐negative cervical cancer.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 84, doi. 10.1002/gcc.22799
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- Article
Molecular characterization of hepatic epithelioid hemangioendothelioma reveals alterations in various genes involved in DNA repair, epigenetic regulation, signaling pathways, and cell cycle control.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 106, doi. 10.1002/gcc.22795
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- Article
Table of Content Volume 59, Number 2, February 2020.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 71, doi. 10.1002/gcc.22770
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- Article
MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 111, doi. 10.1002/gcc.22804
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- Article