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Prenatal Diagnosis|November 1, 1994
Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridizationE Blennow, T H Bui, U Kristoffersson, et al.Human Genetics|December 1, 1992
Complete characterization of a large marker chromosome by reverse and forward chromosome paintingE Blennow, H Telenius, C Larsson, et al.Cytometry|January 1, 1993
Chromatid contamination can impair the purity of flow-sorted metaphase chromosomesH Telenius, D de Vos, E Blennow, et al.Leukemia & Lymphoma|February 1, 1993
DNA image analysis in childhood acute lymphoblastic leukemiaM Czader, A Porwit, S Söderhäll, et al.Journal of Medical Genetics|December 1, 1995
Partial disomy of Xp and the presence of SRY in a phenotypic femaleS Bajalica, E Blennow, A Tşezou, et al.American Journal of Medical Genetics|March 10, 2001
Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomyB M Anderlid, S Sahlén, J Schoumans, et al.Human Genetics|October 1, 1994
Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22Y G Xie, F Y Han, S Bajalica, et al.Molecular Human Reproduction|March 27, 2004
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivationJ Inzunza, S Sahlén, K Holmberg, et al.American Journal of Medical Genetics|April 5, 2000
Molecular cytogenetic characterization and origin of two de novo duplication 9p casesA Tsezou, S Kitsiou, A Galla, et al.European Journal of Haematology|June 26, 2001
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotypingA Nordgren, F Farnebo, B Johansson, et al.Pageof 6