Division of Clinical Genetics

Organisational unit: Division

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  1. Somatic Genetic Variation in Children: from Mosaicism to Cancer

    Anders Valind, 2017 Dec 15, Lund: Lund University: Faculty of Medicine. 58 p.

    Research output: ThesisDoctoral Thesis (compilation)

  2. Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

    Anders Valind, Wessman, S., Pal, N., Jenny Karlsson, Tord Jonson, Sandstedt, B. & David Gisselsson, 2018 Nov 1, In : Pediatric Blood and Cancer. 65, 11, e27301.

    Research output: Contribution to journalArticle

  3. Global binding pattern of the Wilms' tumor gene 1 (WT1) +17AA -KTS isoform in leukemic cells

    Tove Ullmark, Järvstråt, L., Giorgia Montano, Helena Jernmark-Nilsson, Carl Sandén, Karina Vidovic & Urban Gullberg, 2016 Jun 2, In : Cancer Research. 76, 14 Suppl., Abstract nr 2005.

    Research output: Contribution to journalPublished meeting abstract

  4. The gynecological surveillance of women with Lynch syndrome in Sweden.

    Tzortzatos, G., Andersson, E., Soller, M., Askmalm, M. S., Zagoras, T., Georgii-Hemming, P., Lindblom, A., Tham, E. & Mints, M., 2015, In : Gynecologic Oncology. 138, 3, p. 717-722

    Research output: Contribution to journalArticle

  5. Recombinant dermatan sulfate is a potent activator of heparin cofactor II-dependent inhibition of thrombin

    Emil Tykesson, Maccarana, M., Thorsson, H., Liu, J., Anders Malmström, Ulf Ellervik & Gunilla Westergren-Thorsson, 2019, In : Glycobiology. 29, 6, p. 446-451

    Research output: Contribution to journalArticle

  6. Clinical Variability of Waardenburg-Shah Syndrome in Patients With Proximal 13q Deletion Syndrome Including the Endothelin-B Receptor Locus

    Tuysuz, B., Collin, A., Arapoglu, M. & Suyugul, N., 2009, In : American Journal of Medical Genetics. Part A. 149A, 10, p. 2290-2295

    Research output: Contribution to journalArticle

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