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Leukemia|April 1, 1994
Detection of minimal residual disease using fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patientsS J Nylund, T Ruutu, U Saarinen, et al.
Clinical Genetics|June 1, 1987
Pallister-Killian syndrome: cytogenetic and molecular studiesP Peltomäki, S Knuutila, A Ritvanen, et al.
Cancer Genetics and Cytogenetics|February 1, 1985
t(11;19)(q23;p11) in a child with acute T-cell leukemiaS Knuutila, J Rajantie, R Leskinen, et al.
Blood|August 1, 1997
BCL2 overexpression associated with chromosomal amplification in diffuse large B-cell lymphomaO Monni, H Joensuu, K Franssila, et al.
Cancer Genetics and Cytogenetics|April 1, 1984
Critical chromosome rearrangement in acute promyelocytic leukemiaS Knuutila, T Ruutu, R Kovanen, et al.
Cytogenetics and Cell Genetics|January 1, 1995
The human S-adenosylmethionine decarboxylase gene: nucleotide sequence of a pseudogene and chromosomal localization of the active gene (AMD1) and the pseudogene (AMD2)S C Maric, A Crozat, J Louhimo, et al.
British Journal of Haematology|January 1, 1994
Ploidy in bone marrow cells from healthy donors: a MAC (morphology antibody chromosomes) studyM L Larramendy, S J Nylund, M Wessman, et al.
Oncogene|June 6, 2006
DNA copy number amplification profiling of human neoplasmsS Myllykangas, J Himberg, T Böhling, et al.
Genes, Chromosomes & Cancer|May 25, 1999
Among numerous DNA copy number changes, losses of chromosome 13 are highly recurrent in plasmacytomaY Aalto, S Nordling, A H Kivioja, et al.
Experimental Hematology|December 1, 1995
Myeloid lineage involvement in acute lymphoblastic leukemia: a morphology antibody chromosomes (MAC) studyM Larramendy, W el-Rifai, U Saarinen, et al.
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