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Cytogenetics and Cell Genetics|January 1, 1986
Determination of the DNA content of human chromosomes by flow cytometryP Harris, E Boyd, B D Young, et al.Oncogene|June 11, 1999
Molecular analysis of an unstable genomic region at chromosome band 11q23 reveals a disruption of the gene encoding the alpha2 subunit of platelet-activating factor acetylhydrolase (Pafah1a2) in human lymphomaN Lecointe, J Meerabux, M Ebihara, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1981
High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometryB D Young, M A Ferguson-Smith, R Sillar, et al.Journal of Molecular Endocrinology|March 1, 1989
Amplification or rearrangement of the beta-human chorionic gonadotrophin (beta-hCG)--human LH gene cluster is not responsible for the ectopic production of beta-hCG by bladder tumour cellsR K Iles, B H Czepulkowski, B D Young, et al.Molecular and Cellular Endocrinology|January 1, 1982
Ploidy and progesterone-receptor distribution in flow-sorted deciduomal nucleiK N McConnell, R G Sillar, B D Young, et al.Cancer Genetics and Cytogenetics|February 15, 2001
The use of multicolor fluorescence technologies in the characterization of prostate carcinoma cell lines: a comparison of multiplex fluorescence in situ hybridization and spectral karyotyping dataJ C Strefford, D M Lillington, B D Young, et al.Current Protocols in Cytometry|September 5, 2008
Advanced preparative techniques to establish probes for molecular cytogeneticsJ Stap, J A Aten, D Lillington, et al.Human Molecular Genetics|July 11, 2000
The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombinationA S Hill, N J Foot, T L Chaplin, et al.Blood|September 1, 1987
Molecular analysis of relapse in chronic myeloid leukemia after allogeneic bone marrow transplantationT S Ganesan, G L Min, J M Goldman, et al.Journal of Medical Genetics|February 1, 1991
The origin of a morphologically unidentifiable human supernumerary minichromosome traced through sorting, molecular cloning, and in situ hybridisationE Raimondi, L Ferretti, B D Young, et al.Pageof 14