Maria Planck
Department of Oncology
University Hospital
Sweden
Name/email consistency: high
- Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer. Planck, M., Halvarsson, B., Pålsson, E., Hallén, M., Ekelund, M., Pålsson, B., Baldetorp, B., Nilbert, M. Cancer Genet. Cytogenet. (2002)
- High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum. Planck, M., Rambech, E., Möslein, G., Müller, W., Olsson, H., Nilbert, M. Cancer (2002)
- Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation. Planck, M., Wenngren, E., Borg, A., Olsson, H., Nilbert, M. Genes. Chromosomes. Cancer (2000)
- hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden. Planck, M., Koul, A., Fernebro, E., Borg, A., Kristoffersson, U., Olsson, H., Wenngren, E., Mangell, P., Nilbert, M. Int. J. Cancer (1999)