Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. Provision of genetic service in Europe: current practices and issues.

    Aymé, S., Cassiman, J-J., Coviello, D., Evers-Kiebooms, G., Kääriäinen, H., Ulf Kristoffersson, Pembrey, M., Schmidtke, J., ten Kate, L. & Tranebjaerg, L., 2003, I : European Journal of Human Genetics. 11, s. 900-902

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. An excess of chromosome 1 breakpoints in male infertility.

    Bache, I., Van Assche, E., Cingoz, S., Bugge, M., Tümer, Z., Hjorth, M., Lundsteen, C., Lespinasse, J., Winther, K., Niebuhr, A., Kalscheuer, V., Liebaers, I., Bonduelle, M., Tournaye, H., Ayuso, C., Barbi, G., Blennow, E., Bourrouillou, G., Brondum-Nielsen, K., Bruun-Petersen, G. & 39 andra, Croquette, M-F., Dahoun, S., Dallapiccola, B., Davison, V., Delobel, B., Duba, H-C., Duprez, L., Ferguson-Smith, M., FitzPatrick, D. R., Grace, E., Hansmann, I., Hultén, M., Jensen, P. KA., Jonveaux, P., Ulf Kristoffersson, Lopez-Pajares, I., McGowan-Jordan, J., Murken, J., Orera, M., Parkin, T., Passarge, E., Ramos, C., Rasmussen, K., Schempp, W., Schubert, R., Schwinger, E., Shabtai, F., Smith, K., Stallings, R., Stefanova, M., Tranebjerg, L., Turleau, C., van der Hagen, C. B., Vekemans, M., Kokalj Vokac, N., Wagner, K., Wahlstroem, J., Zelante, L. & Tommerup, N., 2004, I : European Journal of Human Genetics. 12, 12, s. 993-1000

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol

    Barbany, G., Andersen, M. K., Autio, K., Borgstrom, G., Franco, L. C., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Bertil Johansson, Johannsson, J. H., Kjeldsen, E., Nordgren, A., Palmqvist, L. & Forestier, E., 2012, I : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 36, 7, s. 936-938

    Forskningsoutput: TidskriftsbidragLetter

  4. Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.

    Barbouti, A., Bertil Johansson, Mattias Höglund, Mauritzson, N., Strömbeck, B., Nilsson, P-G., Tanke, H. J., Hagemeijer, A., Felix Mitelman & Thoas Fioretos, 2002, I : Genes, Chromosomes and Cancer. 35, 2, s. 127-137

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.

    Barbouti, A., Stankiewicz, P., Nusbaum, C., Cuomo, C., Cook, A., Mattias Höglund, Bertil Johansson, Hagemeijer, A., Park, S-S., Felix Mitelman, Lupski, J. R. & Thoas Fioretos, 2004, I : American Journal of Human Genetics. 74, 1, s. 1-10

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia

    Barbouti, A., 2004, Anette Welin, Academic Secretary, Department of Clinical Genetics, Lund University Hospital, SE-221 85 Lund, Sweden,. 100 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  7. Tumor karyotype predicts clinical outcome in colorectal cancer patients

    Bardi, G., Fenger, C., Bertil Johansson, Felix Mitelman & Heim, S., 2004, I : Journal of Clinical Oncology. 22, 13, s. 2623-2634

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift