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British Journal of Haematology|May 31, 2001
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemiaH Starke, M Raida, V Trifonov, et al.International Journal of Oncology|February 17, 2000
Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemiasA Heller, I Chudoba, C Bleck, et al.Cytogenetic and Genome Research|December 28, 2007
DNA degradation during maturation of erythrocytes - molecular cytogenetic characterization of Howell-Jolly bodiesT Felka, J Lemke, C Lemke, et al.Cytogenetic and Genome Research|April 17, 2003
Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosisU Claussen, S Michel, P Mühlig, et al.Cytogenetics and Cell Genetics|December 22, 2000
Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and foxN B Rubtsov, T V Karamisheva, N M Astakhova, et al.Genes, Chromosomes & Cancer|April 3, 2001
Genetic imbalances in 26 cases of penile squamous cell carcinomaG Alves, A Heller, W Fiedler, et al.Genes, Chromosomes & Cancer|October 2, 2001
Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1S Scheil, S Brüderlein, T Liehr, et al.Cytogenetic and Genome Research|March 9, 2004
A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected]U Grasshoff, S Singer, T Liehr, et al.American Journal of Medical Genetics. Part A|July 29, 2003
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]S Sauter, G von Beust, P Burfeind, et al.Cytogenetic and Genome Research|November 12, 2003
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formationI Bartels, G Schlueter, T Liehr, et al.Pageof 26