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2 documents found
1: Title: Fusion of the HMGA2 and C9orf92 genes in myolipoma with t(9;12)(p22;q14).
Authors: Panagopoulos, Ioannis, et.al. .
Journal: Diagnostic pathology (Diagn Pathol), Vol. 11, 2016 .
Snippet: Molecular genetic analysis showed that the translocation resulted in fusion of HMGA2 with the C9orf92 gene (from 9p22).
Affiliation: Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, P.O. Box 4953, Nydalen, NO-0424, Oslo, Norway. ioannis.panagopoulos@rr-research.no. Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Oslo, Norway. ioannis.panagopoulos@rr-research.no. Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, P.O. Box 4953, Nydalen, NO-0424, Oslo, Norway. ludmila.gorunova@rr-research.no. Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Oslo, Norway. ludmila.gorunova@rr-research.no. Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, P.O. Box 4953, Nydalen, NO-0424, Oslo, Norway. Antonio.Agostini@rr-research.no. Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Oslo, Norway. Antonio.Agostini@rr-research.no. Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway. sbkori@ous-hf.no. Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway. BOB@ous-hf.no. Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, P.O. Box 4953, Nydalen, NO-0424, Oslo, Norway. sverre.heim@medisin.uio.no. Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Oslo, Norway. sverre.heim@medisin.uio.no. Faculty of Medicine, University of Oslo, Oslo, Norway. sverre.heim@medisin.uio.no. .
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2: Title: The clinical and pathological phenotypes of frontotemporal dementia with C9ORF72 mutations.
Authors: Liu, Ying, et.al. .
Journal: Journal of the neurological sciences (J Neurol Sci), Vol. 335 (1-2): 26-35, 2013 .
Snippet: An expanded hexanucleotide repeat in the chromosome 9 open reading frame 72 (C9ORF72), on chromosome 9p21, has recently been identified as a major cause of familial frontotemporal dementia (FTD).
Affiliation: Department of Neurology, Qingdao Municipal Hospital, Dalian Medical University, China. .
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