PDF) The recurrent chromosomal translocation t(12;18)(q14~15;q12~21) causes the fusion gene HMGA2-SETBP1 and HMGA2 expression in lipoma and osteochondrolipoma
PLOS ONE: Novel KAT6B-KANSL1 Fusion Gene Identified by RNA Sequencing in Retroperitoneal Leiomyoma with t(10;17)(q22;q21)
PDF) Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification
PDF) DEK-NUP214-Fusion Identified by RNA-Sequencing of an Acute Myeloid Leukemia with t(9;12)(q34;q15)
Digital Public Defence: Synne Torkildsen - Institute of Clinical Medicine
Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity | Oncotarget
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation | Anticancer Research
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
PDF) An Unbalanced Chromosome Translocation Between 7p22 and 12q13 Leads to ACTB-GLI1 Fusion in Pericytoma
PDF) Interstitial Deletions Generating Fusion Genes
PDF) Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21)
PDF) Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
PDF) Recurrent Fusion of the GRB2 Associated Binding Protein 1 ( GAB1 ) Gene With ABL Proto-oncogene 1 ( ABL1 ) in Benign Pediatric Soft Tissue Tumors
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) Genetic Characterization of Myoid Hamartoma of the Breast
Genetic Characterization of Myoid Hamartoma of the Breast | Cancer Genomics & Proteomics
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) Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
PDF) Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma
MGMT promoter methylation is a rare epigenetic change in malignant effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
Institute for Cancer Genetics and Informatics - ICGI - Home | Facebook
The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas | Scientific Reports
PDF) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
