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N Mandahl

Showing results (31-40 of 336) with videos related to

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Hereditas|January 1, 1977
Experimental elimination and recovery of double minute chromosomes in malignant cell populationsG Levan, N Mandahl, B O Bengtsson, et al.
Journal of the Neurological Sciences|March 1, 1991
Increased frequency of chromosome aberrations in long-term cultured cerebrospinal fluid lymphocytes of patients with multiple sclerosisM Sandberg-Wollheim, U Kristoffersson, N Mandahl, et al.
Cancer Genetics and Cytogenetics|January 1, 1987
Late appearing 5q--marker in refractory anemiaS Heim, R Billström, U Kristoffersson, et al.
Leukemia|January 1, 1988
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemiaS Heim, U Kristoffersson, N Mandahl, et al.
Cancer Genetics and Cytogenetics|July 1, 1989
Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcomaN Mandahl, S Heim, A Rydholm, et al.
Genes, Chromosomes & Cancer|June 22, 2000
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasiaD Gisselsson, N Mandahl, E Pålsson, et al.
European Journal of Haematology|September 1, 1990
Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndromeR Billström, S Heim, U Kristoffersson, et al.
Genes, Chromosomes & Cancer|April 1, 1994
MDM2 gene amplification correlates with ring chromosome in soft tissue tumorsM Nilbert, A Rydholm, H Willén, et al.
Clinical & Experimental Metastasis|September 1, 1993
Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomasC Orndal, N Mandahl, H Willén, et al.
British Journal of Cancer|May 27, 2004
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomasD Gisselsson, L Gorunova, M Höglund, et al.
Pageof 34

Showing results (31-40 of 336) with videos related to

Sort By:
Pageof 34
Hereditas|January 1, 1977
Experimental elimination and recovery of double minute chromosomes in malignant cell populationsG Levan, N Mandahl, B O Bengtsson, et al.
Journal of the Neurological Sciences|March 1, 1991
Increased frequency of chromosome aberrations in long-term cultured cerebrospinal fluid lymphocytes of patients with multiple sclerosisM Sandberg-Wollheim, U Kristoffersson, N Mandahl, et al.
Cancer Genetics and Cytogenetics|January 1, 1987
Late appearing 5q--marker in refractory anemiaS Heim, R Billström, U Kristoffersson, et al.
Leukemia|January 1, 1988
Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemiaS Heim, U Kristoffersson, N Mandahl, et al.
Cancer Genetics and Cytogenetics|July 1, 1989
Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcomaN Mandahl, S Heim, A Rydholm, et al.
Genes, Chromosomes & Cancer|June 22, 2000
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasiaD Gisselsson, N Mandahl, E Pålsson, et al.
European Journal of Haematology|September 1, 1990
Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndromeR Billström, S Heim, U Kristoffersson, et al.
Genes, Chromosomes & Cancer|April 1, 1994
MDM2 gene amplification correlates with ring chromosome in soft tissue tumorsM Nilbert, A Rydholm, H Willén, et al.
Clinical & Experimental Metastasis|September 1, 1993
Cytogenetic evolution in primary tumors, local recurrences, and pulmonary metastases of two soft tissue sarcomasC Orndal, N Mandahl, H Willén, et al.
British Journal of Cancer|May 27, 2004
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomasD Gisselsson, L Gorunova, M Höglund, et al.
Pageof 34