MGMT promoter methylation is a rare epigenetic change in malignant effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library
PDF) Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
PDF) Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21)
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
PDF) NDRG1-PLAG1 and TRPS1-PLAG1 fusion genes in chondroid syringoma
The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas | Scientific Reports
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Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22‐translocation - Panagopoulos - 2013 - Genes, Chromosomes and Cancer - Wiley Online Library
PDF) Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma
PDF) Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
Monosomy 13 in Mammary Myofibroblastoma | Anticancer Research
PLOS ONE: The “Grep” Command But Not FusionMap, FusionFinder or ChimeraScan Captures the CIC-DUX4 Fusion Gene from Whole Transcriptome Sequencing Data on a Small Round Cell Tumor with t(4;19)(q35;q13)
Monosomy 13 in Mammary Myofibroblastoma | Anticancer Research
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma - Micci - 2017 - Genes, Chromosomes and Cancer - Wiley Online Library
PDF) FOS-ANKH and FOS-RUNX2 fusion genes in osteoblastoma
PDF) Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies | Geir Tjønnfjord, Arne Kolstad, and Ioannis Panagopoulos - Academia.edu
Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation | Anticancer Research
PDF) Genetic Characterization of Myoid Hamartoma of the Breast
Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook
PDF) t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma | Bodil Bjerkehagen - Academia.edu
Digital Public Defence: Synne Torkildsen - Institute of Clinical Medicine
PDF) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook
PDF) FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
PDF) Characterisation of genomic translocation breakpoints and identification of an alternative TCF3 / PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias | Ingrid Øra - Academia.edu
PDF) Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification
