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American Journal of Medical Genetics. Supplement|January 1, 1990
Trisomy 21 in neoplastic cellsF Mitelman, S Heim, N MandahlHereditas|January 1, 1989
In situ hybridization localizes the human type II alpha 1 collagen gene (COL2A1) to 12q13K Arheden, N Mandahl, S Heim, et al.Pediatric Hematology and Oncology|July 1, 1994
Cytogenetic analysis in the examination of solid tumors in childrenF Mertens, N Mandahl, F Mitelman, et al.Cancer Genetics and Cytogenetics|October 1, 1989
The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15K Arheden, N Mandahl, S Heim, et al.Cancer Genetics and Cytogenetics|June 1, 1989
No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24)K Arheden, M Nilbert, S Heim, 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.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.Cytogenetics and Cell Genetics|January 1, 1989
Genetic convergence during serial in vitro passage of a polyclonal squamous cell carcinomaS Heim, M Caron, Y Jin, et al.Cancer Genetics and Cytogenetics|October 15, 1989
Structural chromosome aberrations in an adamantinomaN Mandahl, S Heim, A Rydholm, et al.Pageof 87