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Cancer Genetics and Cytogenetics|May 1, 1990
Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovaryT Pejovic, S Heim, N Mandahl, et al.
Cancer Genetics and Cytogenetics|January 1, 1988
Unique karyotypic abnormalities in a squamous cell carcinoma of the larynxY S Jin, N Mandahl, S Heim, et al.
Leukemia|December 17, 2005
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42K Paulsson, A N Békássy, T Olofsson, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Assignment of the rat genes coding for phenylalanine hydroxylase (PAH), tyrosine aminotransferase (TAT), and pyruvate kinase (PKL) to chromosomes 7, 19, 2, respectivelyM C Fulchignoni-Lataud, M C Weiss, C Szpirer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Assignment of the rat genes coding for alpha 1-antitrypsin (PI), phosphoenolpyruvate carboxykinase (PEPCK), alcohol dehydrogenase (ADH), and fructose-1,6-bisphosphatase (FDP)M C Fulchignoni-Lataud, J Szpirer, G Levan, et al.
Genes, Chromosomes & Cancer|May 29, 2000
Genomewide assessment of genetic alterations in DMBA-induced rat sarcomas: cytogenetic, CGH, and allelotype analyses reveal recurrent DNA copy number changes in rat chromosomes 1, 2, 4, and 7A Walentinsson, A Sjöling, K Helou, et al.
Experimental Hematology|April 21, 1999
Establishment and characterization of a mouse strain (TLL) that spontaneously develops T-cell lymphomas/leukemiaB Eriksson, A S Johansson, G Roos, et al.
European Journal of Haematology|March 25, 1999
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomasM Jerkeman, B Johansson, M Akerman, et al.
Scandinavian Journal of Work, Environment & Health|December 1, 1979
Increased frequency of chromosome aberrations in workers exposed to styreneB Högstedt, K Hedner, E Mark-Vendel, et al.
Genes, Chromosomes & Cancer|January 27, 1998
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2M Höglund, L Gorunova, A Andrén-Sandberg, et al.
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