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Clinical Genetics|July 1, 1987
Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformationsF Mertens, B Johansson, M Forslund, et al.American Journal of Medical Genetics|April 1, 1988
Duplication 18p with mild influence on the phenotypeB Johansson, F Mertens, L Palm, et al.Genes, Chromosomes & Cancer|October 1, 1996
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcomaI Panagopoulos, P Aman, F Mertens, 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.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.Cancer Genetics and Cytogenetics|June 1, 1995
Clonal karyotypic evolution in a pediatric neurofibrosarcomaF Mertens, S Heim, C M Kullendorff, et al.Genes, Chromosomes & Cancer|November 20, 1997
BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusionP Andreasson, B Johansson, M Carlsson, et al.European Journal of Haematology|January 1, 1996
NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16)I Panagopoulos, P Aman, B Johansson, et al.European Journal of Haematology|July 1, 1997
Poor survival in t(8;21) (q22;q22)-associated acute myeloid leukaemia with leukocytosisR Billström, B Johansson, T Fioretos, et al.Genes, Chromosomes & Cancer|January 1, 1994
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostosesF Mertens, A Rydholm, A Kreicbergs, et al.Pageof 152