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Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.American Journal of Medical Genetics|October 20, 2000
Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimenB Fritz, S Greber-Platzer, T Frischer, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|October 23, 1997
Iodine-123-alpha-methyl tyrosine in gliomas: correlation with cellular density and proliferative activityT Kuwert, S Probst-Cousin, B Woesler, et al.American Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVSJ Bernert, I Bartels, G Gatz, et al.Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1993
Monoclonal antibody MS-44B reacts with human dendritic, glial and endothelial cells: differential expression of MS-44B antigen by epidermal dendritic cells and by MS-1+ splenic sinusoidal endothelial cells. An immunohistological studyS Goerdt, E B Bröcker, K Redmann, et al.Brain Pathology (Zurich, Switzerland)|October 1, 1995
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.European Journal of Human Genetics : EJHG|July 21, 2001
Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortionsB Fritz, C Hallermann, J Olert, et al.Annales De Genetique|January 1, 1991
No evidence of mutations in four candidate genes for male sex determination/differentiation in sex-reversed XY females with campomelic dysplasiaC Ebensperger, R J Jäger, U Lattermann, et al.American Journal of Medical Genetics|May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatallyP Miny, B Koppers, B Dworniczak, et al.Pageof 22