Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation | Anticancer Research
PDF) Cryptic FUS-ERG fusion identified by RNA-sequencing in childhood acute myeloid leukemia
PLOS ONE: Novel KAT6B-KANSL1 Fusion Gene Identified by RNA Sequencing in Retroperitoneal Leiomyoma with t(10;17)(q22;q21)
PDF) FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
2019 CancerGenomicProteomics WWTR1 FOSB | PDF | Dna Sequencing | Promoter (Genetics)
t(12;13)(q14;q31) leading to HMGA2 upregulation in acute myeloid leukaemia - Nyquist - 2012 - British Journal of Haematology - Wiley Online Library
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma - Micci - 2017 - Genes, Chromosomes and Cancer - Wiley Online Library
Institute for Cancer Genetics and Informatics - ICGI - Home | Facebook
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) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report
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.
PDF) FOS-ANKH and FOS-RUNX2 fusion genes in osteoblastoma
Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook
PDF) NDRG1-PLAG1 and TRPS1-PLAG1 fusion genes in chondroid syringoma
PDF) Interstitial Deletions Generating Fusion Genes
MGMT promoter methylation is a rare epigenetic change in malignant effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library
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
PDF) t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma | Bodil Bjerkehagen - Academia.edu
Monosomy 13 in Mammary Myofibroblastoma | 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) Molecular Genetic Characterization of Acute Myeloid Leukemia With Trisomy 4 as the Sole Chromosome Abnormality
