Primary spinal intradural mesenchymal chondrosarcoma with detection of fusion gene HEY1-NCOA2: A paediatric case report and review of the literature

por ANDERSSON, CAROLA, ÖSTERLUNDH, GUSTAF, ENLUND, FREDRIK, KINDBLOM, LARS-GUNNAR, HANSSON, MAGNUS
Publicado 2014

A Founder Mutation of the BRCA1-Gene in Western Sweden

por Einbeigi, Zakaria, Kindblom, Jeane, Kindblom, Lars-Gunnar, Martinsson, Tommy, Suurkula, Mart, Wahlström, Jan, Wallgren, Arne, Karlsson, Per
Publicado 1999

Somatic mosaic IDH1 or IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

por Pansuriya, Twinkal C., van Eijk, Ronald, Adamo, Pio d', van Ruler, Maayke A.J.H., Kuijjer, Marieke L., Oosting, Jan, Cleton-Jansen, Anne-Marie, van Oosterwijk, Jolieke G., Verbeke, Sofie L.J., Meijer, Daniëlle, van Wezel, Tom, Nord, Karolin H., Sangiorgi, Luca, Toker, Berkin, Liegl-Atzwanger, Bernadette, San-Julian, Mikel, Sciot, Raf, Limaye, Nisha, Kindblom, Lars-Gunnar, Daugaard, Soeren, Godfraind, Catherine, Boon, Laurence M., Vikkula, Miikka, Kurek, Kyle C., Szuhai, Karoly, French, Pim J., Bovée, Judith V.M.G.
Publicado 2011