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Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors:  site-specific cytogenetic evolution as evidence of pathogenetic  heterogeneity | Oncotarget
Cytogenetic and molecular analyses of 291 gastrointestinal stromal tumors: site-specific cytogenetic evolution as evidence of pathogenetic heterogeneity | Oncotarget

Digital Public Defence: Synne Torkildsen - Institute of Clinical Medicine
Digital Public Defence: Synne Torkildsen - Institute of Clinical Medicine

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) 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
PDF) Genetic Characterization of Myoid Hamartoma of the Breast

PDF) FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation  in acute lymphoblastic leukemia
PDF) FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia

Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook
Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook

MGMT promoter methylation is a rare epigenetic change in malignant  effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library
MGMT promoter methylation is a rare epigenetic change in malignant effusions - Brunetti - 2020 - Cytopathology - Wiley Online Library

PDF) Molecular Genetic Characterization of Acute Myeloid Leukemia With  Trisomy 4 as the Sole Chromosome Abnormality
PDF) Molecular Genetic Characterization of Acute Myeloid Leukemia With Trisomy 4 as the Sole Chromosome Abnormality

PDF) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22)  chromosome translocation in acute myeloid leukemia: A case report
PDF) RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report

PDF) NDRG1-PLAG1 and TRPS1-PLAG1 fusion genes in chondroid syringoma
PDF) NDRG1-PLAG1 and TRPS1-PLAG1 fusion genes in chondroid syringoma

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) The recurrent chromosomal translocation t(12;18)(q14~15;q12~21) causes the fusion gene HMGA2-SETBP1 and HMGA2 expression in lipoma and osteochondrolipoma

Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook
Institute for Cancer Genetics and Informatics - ICGI - Posts | Facebook

Institute for Cancer Genetics and Informatics - ICGI - Home | Facebook
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) Recurrent Fusion of the GRB2 Associated Binding Protein 1 ( GAB1 ) Gene With ABL Proto-oncogene 1 ( ABL1 ) in Benign Pediatric Soft Tissue Tumors

PDF) Molecular cytogenetic characterization of t(14;19)(q32;p13), a new  recurrent translocation in B cell malignancies
PDF) Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies

The microRNA miR-192/215 family is upregulated in mucinous ovarian  carcinomas | Scientific Reports
The microRNA miR-192/215 family is upregulated in mucinous ovarian carcinomas | Scientific Reports

PDF) t(19;22)(q13;q12) Translocation leading to the novel fusion gene  EWSR1-ZNF444 in soft tissue myoepithelial carcinoma | Bodil Bjerkehagen -  Academia.edu
PDF) t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1-ZNF444 in soft tissue myoepithelial carcinoma | Bodil Bjerkehagen - Academia.edu

PDF) Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal  chondrosarcoma
PDF) Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma

Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma - Micci -  2017 - Genes, Chromosomes and Cancer - Wiley Online Library
Fusion of the genes BRD8 and PHF1 in endometrial stromal sarcoma - Micci - 2017 - Genes, Chromosomes and Cancer - Wiley Online Library

PDF) Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma
PDF) Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma

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
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

Monosomy 13 in Mammary Myofibroblastoma | Anticancer Research
Monosomy 13 in Mammary Myofibroblastoma | Anticancer Research

PDF) Interstitial Deletions Generating Fusion Genes
PDF) Interstitial Deletions Generating Fusion Genes

Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal  Translocation | Anticancer Research
Chronic Expanding Hematoma with a t(11;19)(q13;q13) Chromosomal Translocation | Anticancer Research

OUH - Employees
OUH - Employees