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The New England Journal of Medicine|April 3, 1986
Trisomy 12 in B cells of patients with B-cell chronic lymphocytic leukemiaS Knuutila, E Elonen, L Teerenhovi, et al.International Journal of Cancer|April 22, 2024
Cancer-associated fibroblast activation predicts progression, metastasis, and prognosis of cutaneous squamous cell carcinomaJaakko S Knuutila, Pilvi Riihilä, Liisa Nissinen, et al.Cytogenetics and Cell Genetics|December 22, 1998
Optimized mitogen stimulation induces proliferation of neoplastic B cells in chronic lymphocytic leukemia: significance for cytogenetic analysis.The Tampere Chronic Lympocytic Leukemia groupM L Larramendy, S M Siitonen, Y Zhu, et al.Cancer Genetics and Cytogenetics|November 24, 1999
Clinical importance of genomic imbalances in synovial sarcoma evaluated by comparative genomic hybridizationB T Skytting, J Szymanska, Y Aalto, et al.Genes, Chromosomes & Cancer|March 1, 1992
Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignanciesM Tiainen, S Popp, V Parlier, et al.Medical and Pediatric Oncology|December 18, 2001
Loss at 12p detected by comparative genomic hybridization (CGH): association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional studyJ Kanerva, T Niini, K Vettenranta, et al.Cancer Genetics and Cytogenetics|August 1, 1997
No DNA copy number changes in osteochondromas: a comparative genomic hybridization studyM L Larramendy, J Valle, M Tarkkanen, et al.International Journal of Cancer|August 4, 1998
A cloned human germ cell tumor-derived cell line differentiating in cultureJ Tienari, I Reima, M L Larramendy, et al.Cancer Genetics and Cytogenetics|January 20, 2000
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3pF Mertens, M Larramendy, A Gustavsson, et al.Human Mutation|February 12, 2000
A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. OnlineM Wolf, A Hemminki, A Kivioja, et al.Pageof 30