Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity | Oncotarget
Cytogenetic and Molecular Profile of Endometrial Stromal Sarcoma – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
PLOS ONE: Novel KAT6B-KANSL1 Fusion Gene Identified by RNA Sequencing in Retroperitoneal Leiomyoma with t(10;17)(q22;q21)
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) NDRG1-PLAG1 and TRPS1-PLAG1 fusion genes in chondroid syringoma
PDF) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
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)
PDF) Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
Digital Public Defence: Synne Torkildsen - Institute of Clinical Medicine
PDF) Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21)
Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation | Anticancer Research
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
PDF) An Unbalanced Chromosome Translocation Between 7p22 and 12q13 Leads to ACTB-GLI1 Fusion in Pericytoma
PDF) FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
PDF) Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma
Monosomy 13 in Mammary Myofibroblastoma | Anticancer Research
PDF) Interstitial Deletions Generating Fusion Genes
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)
MGMT promoter methylation is a rare epigenetic change in malignant effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library
t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia - Nyquist - 2012 - British Journal of Haematology - Wiley Online Library
PDF) Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
Genetic Characterization of Myoid Hamartoma of the Breast | Cancer Genomics & Proteomics
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
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
